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: HIG FDA class 2

Insufflator, Hysteroscopic

Obstetrics/Gynecology

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The Hysteroscopic Insufflator is a device used to distend the uterine cavity with gas (typically carbon dioxide) during hysteroscopic procedures, creating the space needed for visualization and operative access to the endometrial cavity. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification. The product code is HIG, regulated under 21 CFR 884.1700, within the Obstetrics/Gynecology specialty. It is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)
X-FLO Fluid Management System
Endomat Select, IBS Shaver Software, License
Endomat Select
Fluent Fluid Management System
GYN-Pump PH304
Aquilex Fluid Control System AQL-100S
FluidSmart
THERMEDX FLUID MANAGMENT SYSTEM
HYSTEROSCOPY PUMP HM6
AQUILEX FLUID CONTROL SYSTEM H112
DOLPHIN 3 FLUID MANAGEMENT SYSTEM
THERMEDX PRODIGY FLUID MANAGEMENT SYSTEM, MODELS P1000, P2000
IUR FLUID MANAGEMENT SYSTEM
AQUASENS FLUID MONITORING SYSTEM
HYSTEREOSCOPY PUMP HM4
DOLPHIN II FLUID MANAGEMENT SYSTEM, MODEL DOL-2
AQUASENS FLUID MONITORING SYSTEM
KARL STORZ HYSTEROMAT II
DAVOL HYSTEROSCOPY POUCH DRAPE AND TUBING SET, MODEL OOXXXXO
HYDROFLEX HD HYSTEROSCOPIC DISTENTION SYSTEM,MODEL #'S 0025360, 0025370, 0025000
HYS-SURGIFLATOR 150P
HYDROFLOEX HD HYSTEROSCOPIC DISTENTION SYSTEM
AUTOMATIC ELECTRONIC HYSTEROSCOPIC INSUFFLATOR
HYSTERO CO2-PNEU 2221
KARL STORZ MODEL 203020 20 EQUIMAT
HYS-SURGIMAT
HYS-SURGIFLATOR VP
KSEA DISPOSABLE TUBING SETS FOR THE HAMOU ENDOMAT PUMP
CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
HYS-SURGIFLATOR
THE KARL STORZ HAMOU ENDOMAT
BARD HYSTERO-FLO II PUMP
CONCEPT UNIVERSAL PUMP SYSTEM
HYSTEROMAT(TM) 3700
HYSTEROMED 100
WOM HYSTEROFLATOR OP
7-510-25 HYSTEROMED TUBING KIT
INSUFFLATOR TUBING KIT
THE KARL STORZ 26025UC HAMOU ELEC HYSTEROFLATOR
HYSTEROFLATOR 1500
LM-100/200LOW FLOW INSUFFLATOR
HYSTEROMAT HYSTEROFLATOR HYSTEROSCOPIC INSUFFLATOR
GYN-1500 HYSTEROSCOPIC INUFFLATOR
DAVOL SCOPE IRRIGATION SYSTEM
CONTROLLED DISTENTION IRRIGATION SYSTEM CDIS 200
REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA
HUI MINI-FLEX
HYSTEROFLATOR 2001
DEX-CELL HYSTEROSCOPY FLUID DELIVERY DEVICE

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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