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

Scale, Patient

21 CFR 880.2720 / General Hospital
FDA source (opens on fda.gov)

FRW is the FDA product code for Scale, Patient, a class I device type, regulated under 21 CFR 880.2720. As of , FDA records hold 48 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
FRW
Device name
Scale, Patient
Regulation
21 CFR 880.2720
Device class
Class I
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
48
Ingested recalls
7

Clearances, product code FRW

By decision year
48 clearances under product code FRW with a decision year between 1976 and 1996, 1993 the highest year at 9.
Show the numbers
510(k) clearances under FDA product code FRW by decision year
YearClearances
19761
19781
19791
19823
19832
19842
19854
19861
19876
19905
19915
19923
19939
19941
19953
19961

Applicants with the most clearances

Product code FRW
Applicants holding the most 510(k) clearances under product code FRW
ApplicantClearances
Acme Medical Scale Co.7
Olympic Medical Corp.7
Scale-Tronix, Inc.3
U.S. Medical Corp.3
3M Company2
Apollo Enterprise, Ltd. Co.2
Seca Corp.2
Air-Shields, Inc.1
Alphamed, Inc.1
Arjo-Century, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 95 companies shown, in name order