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

Scale, Platform, Wheelchair

21 CFR 890.3940 / Physical Medicine
FDA source (opens on fda.gov)

INF is the FDA product code for Scale, Platform, Wheelchair, a class I device type, regulated under 21 CFR 890.3940. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
INF
Device name
Scale, Platform, Wheelchair
Regulation
21 CFR 890.3940
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code INF

By decision year
5 clearances under product code INF with a decision year between 1976 and 1993, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code INF by decision year
YearClearances
19761
19871
19881
19911
19931

Applicants with the most clearances

Product code INF
Applicants holding the most 510(k) clearances under product code INF
ApplicantClearances
Acme Medical Scale Co.2
Amigo Sales, Inc.1
Medical Flotation Systems, Inc.1
U.S. Medical Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order