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

Cushion, Wheelchair

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

IMP is the FDA product code for Cushion, 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 one recall.

Classification record

Product code
IMP
Device name
Cushion, 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
1

Clearances, product code IMP

By decision year
2 clearances under product code IMP with a decision year between 1987 and 1989, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IMP by decision year
YearClearances
19871
19891

Applicants with the most clearances

Product code IMP
Applicants holding the most 510(k) clearances under product code IMP
ApplicantClearances
Advantage Credit Services, Inc.1
Clark Pillow Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 160 companies shown, in name order