KNOClass I

Accessories, Wheelchair

21 CFR 890.3910 / Physical Medicine

KNO is the FDA product code for Accessories, Wheelchair, a class I device type, regulated under 21 CFR 890.3910. As of 2026-09-10, FDA records hold 35 510(k) clearances under this code, the most recent dated 1987-02-26, and 2 recalls.

Classification record

Product code: KNO
Device name: Accessories, Wheelchair
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: 35
Ingested recalls: 2

Clearances, product code KNO

By decision year

35 clearances under product code KNO with a decision year between 1976 and 1987, 1978 the highest year at 8.

Show the numbers

510(k) clearances under FDA product code KNO by decision year
Year	Clearances
1976	4
1978	8
1979	2
1980	4
1981	6
1982	7
1983	3
1987	1

Applicants with the most clearances

Product code KNO

Applicants holding the most 510(k) clearances under product code KNO
Applicant	Clearances
Fred Sammons, Inc.	25
Orthopedic Equipment Co., Inc.	4
Skil-Care Corp.	2
Danek Medical, Inc.	1
Mizuho Orthopedic Systems Inc	1
Pryor Products	1
Redman, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 212 companies shown, in name order