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

Footrest, Wheelchair

21 CFR 890.3920 / Physical Medicine
FDA source (opens on fda.gov)

IMM is the FDA product code for Footrest, Wheelchair, a class I device type, regulated under 21 CFR 890.3920. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IMM
Device name
Footrest, Wheelchair
Regulation
21 CFR 890.3920
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code IMM

By decision year
2 clearances under product code IMM with a decision year between 1982 and 1989, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IMM by decision year
YearClearances
19821
19891

Applicants with the most clearances

Product code IMM
Applicants holding the most 510(k) clearances under product code IMM
ApplicantClearances
Fred Sammons, Inc.1
Union Industrial Co., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 61 companies shown, in name order