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

Components, Wheelchair

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

KNN is the FDA product code for Components, Wheelchair, a class I device type, regulated under 21 CFR 890.3920. As of , FDA records hold 64 510(k) clearances under this code, the most recent dated , and 11 recalls.

Classification record

Product code
KNN
Device name
Components, 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
64
Ingested recalls
11

Clearances, product code KNN

By decision year
64 clearances under product code KNN with a decision year between 1977 and 2022, 1991 the highest year at 11.
Show the numbers
510(k) clearances under FDA product code KNN by decision year
YearClearances
19771
19781
19811
19823
19837
19841
19867
19872
19887
19893
19903
199111
19924
19936
19946
20221

Applicants with the most clearances

Product code KNN
Applicants holding the most 510(k) clearances under product code KNN
ApplicantClearances
Pin Dot Products, Inc.10
Berkeley Electric Wheelchair Co.5
Foley & Lardner4
Fred Sammons, Inc.4
Rolcontrol Products, Co., Inc.4
Labac Systems, Inc.3
Special Health Systems, Ltd.3
A & C Medical Supply1
Artec Environmental Monitoring Division1
Biomedical Horizons, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 135 companies shown, in name order