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

Restraint, Wheelchair, Non-Protective

21 CFR 890.3910 / Physical Medicine
FDA source (opens on fda.gov)

KID is the FDA product code for Restraint, Wheelchair, Non-Protective, a class I device type, regulated under 21 CFR 890.3910. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KID
Device name
Restraint, Wheelchair, Non-Protective
Regulation
21 CFR 890.3910
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
7
Ingested recalls
0

Clearances, product code KID

By decision year
7 clearances under product code KID with a decision year between 1980 and 1997, 1996 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KID by decision year
YearClearances
19801
19963
19973

Applicants with the most clearances

Product code KID
Applicants holding the most 510(k) clearances under product code KID
ApplicantClearances
DeRoyal Industries, Inc.3
Skil-Care Corp.3
Jefferson Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 40 companies shown, in name order