510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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FNGClass II

Lift, Patient, Ac-Powered

21 CFR 880.5500 / General Hospital
FDA source (opens on fda.gov)

FNG is the FDA product code for Lift, Patient, Ac-Powered, a class II device type, regulated under 21 CFR 880.5500. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and 23 recalls.

Classification record

Product code
FNG
Device name
Lift, Patient, Ac-Powered
Regulation
21 CFR 880.5500
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
21
Ingested recalls
23

Clearances, product code FNG

By decision year
21 clearances under product code FNG with a decision year between 1980 and 2012, 1985 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FNG by decision year
YearClearances
19802
19812
19853
19863
19891
19903
19912
19931
19942
20041
20121

Applicants with the most clearances

Product code FNG
Applicants holding the most 510(k) clearances under product code FNG
ApplicantClearances
Century Manufacturing Co.5
Bomdal Medical Equipment, Inc.2
Arjo-Century, Inc.1
Arylift, Inc.1
Barrier Free Lifts, Inc.1
Columbus Mckinnon Corp.1
D.T. Davis Enterprises Ltd.1
D.T. Davis Enterprises Ltd. T/A Hovertech Int'L1
Henry Enterprises, Inc.1
Independent Transfer Equipment Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 57 companies shown, in name order