Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: IRP FDA class 2

Massager, Powered Inflatable Tube

Physical Medicine

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A powered inflatable tube massager is a device that uses air-filled inflatable tubes or bladders, powered by a pump, to apply cyclical pressure and massage to body areas for therapeutic purposes such as improving circulation and reducing muscle tension. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IRP, regulated under 21 CFR 890.5650, within the Physical Medicine medical specialty. This device is eligible for third party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Cryo And Thermo Therapy System
Cryo Sport 2.0 (AVA 501)
Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)
Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air Pressure Therapy System (VU-IPC4X)
Hot and Cold Compression System (A02-C-032)
Cryopush Cold Compression Device (A02-P-001)
Hand Massager (SM004D)
Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507)
AIR COMPRESSION BOOTS 1018195,1018196
Cryon-X Cold Compression
Normatec Elite Hip
Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)
Compression Therapy Device (LGT-2210DS)
Intermittent pressure compression system (Compression Pump PT1005A; Leg Compression Cuffs; L-1001S, L-1001L, L-1001XL, L-1001XXL, L-1001XXXL)
ZT Clinic (MG675A); ZT Cube (ZC3) (MG465A); Z-ONE (MG455A)
Air Compression Leg Massager (UM605, UM606, UM607, UM608,UM609,UM610, UM611, UM617)
Air Compression Leg Massager (K-705)
Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)
Game Ready system (550500-04); Game Ready Control Unit (550550-04); Game Ready Full Leg Boot Wrap - Medium (590923-04); Game Ready Full Leg Boot Wrap - Large (590922-04); Game Ready C-T Spine Wrap (590502-04); Game Ready Half Leg Boot (590906-04); Game Ready Back Wrap (590500-04); Game Ready Hand/Wrist Wrap (590811-04); Game Ready Flexed Elbow Wrap (590903-04); Game Ready Straight Elbow Wrap (590200-04); Game Ready Shoulder Wrap, Medium, Right (590422-04); Game Ready Shoulder Wrap, La
Air Pressure Therapy System
SACS PRO
Leg Massager (Models:RP-ALM070H, RP-ALM071H)
Air Pressure Therapy System (VU-IPC04B)
Xrecovery (XR-001)
Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)
Air compression Leg Massager (MM0520, MM0521, MM0522)
JetBoots PRO Plus
Air compression leg massager
Air Pressure Therapy System (Model:VU-IPC4M)
Cold Compression
Normatec Elite
Cold Compression Wrap Pro
FLOWpresso
Air Compression Recovery System
Cold/Hot Compression
Air Compression Therapy Recovery System (model: MF-AWI, MF-AWI.LED.A-801, MF-AWI.LED.B-801, MF-AWI.OLED.A-601, MF-AWI.LED.A-601, MF-AWI.LED.B-601, MF-AWI.OLED.A-401, MF-AWI.LED.A-401, MF-AWI.LED.B-401)
Therm-X
LF900
Ballancer Platinum (1222)
Air Compression Leg Massager (model: EMK-701)
Leg and Foot Air Wave Pressure Therapy Device
Cryo-Thermo Compression Device (FGK002)
Leg Massager RF-ALM070
Air Compression Leg Massager (Model: LY-670D)
YY-A02-B Overlapped Compression Therapy
Cryopush Cold Compression Device
Aquilo Sports CCT1500 System
Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)
Powered Inflatable Tube Massager - SLIM UP DRAIN
Normatec Go

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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