Product Code: FNG FDA class 2 21 CFR 880.5500

Lift, Patient, Ac-Powered

General Hospital

The AC-Powered Patient Lift is an electrically powered device used in hospital and care settings to safely lift and transfer patients who cannot bear their own weight, reducing manual handling strain and fall risk. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket notification. The product code is FNG, regulated under 21 CFR 880.5500 in the General Hospital specialty.

510(k)s
21
FEI Numbers
58
Registration Numbers
58
Unique Applicants
16
Years Active
32

Basic Information

Product Code
FNG
Device Class
FDA class 2
Regulation Number
880.5500
Medical Specialty
General Hospital
Review Panel
HO
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

Loading...

Related 510(k) Clearances

This FDA classification is associated with 21 510(k) clearances via K numbers.

K Number Device Name
K121287 HT-WEDGE
K041503 HOVERJACK AIR PATIENT LIFT DEVICE
K940872 PATIENT SUPPORT SYSTEM
K935351 A.C. POWER PATIENT LIFT
K926411 SAF-LIFT/SAF-KARY
K912769 PATIENT LIFT AND TRANSPORT
K905414 MANGAR BOOSTER
K895677 THE MURRAY MOBILIFT(TM)
K903723 BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F
K896848 LIFT MASTER PATIENT LIFT
K885270 PERSONAL TRANSFER SYSTEM
K862147 BOMDAL STANDARD LIFT
K862146 BOMDAL TRAVELMASTER LIFT
K854058 PK-AC POWERED PATIENT MANUPULATING DEVICE
K854120 MURRAY CHAIR LIFT
K844872 CENTURY SCALE
K844871 CENTURY SAF-LIFT SCALE
K811900 CENTURY SAF-LIFT & SAF-KARY
K811901 CENTURY BATHING SYSTEM
K802780 JACKSON HYDRO SYSTEM
K801933 DRUALIFT 500

FEI Numbers

This FDA classification entry is associated with 58 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 58 registration numbers. Click on an entry to view related FDA registrations.