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

Device, Patient Transfer, Powered

21 CFR 880.6775 / General Hospital
FDA source (opens on fda.gov)

FRZ is the FDA product code for Device, Patient Transfer, Powered, a class II device type, regulated under 21 CFR 880.6775. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
FRZ
Device name
Device, Patient Transfer, Powered
Regulation
21 CFR 880.6775
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
5
Ingested recalls
2

Clearances, product code FRZ

By decision year
5 clearances under product code FRZ with a decision year between 1984 and 2013, 1984 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FRZ by decision year
YearClearances
19843
19921
20131

Applicants with the most clearances

Product code FRZ
Applicants holding the most 510(k) clearances under product code FRZ
ApplicantClearances
American Invalift Corp.1
Diacor, Inc.1
Lancer Assoc.1
Lehigh Consolidated Industries1
R & D Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 54 companies shown, in name order