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

Board, Scooter, Prone

21 CFR 890.5370 / Physical Medicine
FDA source (opens on fda.gov)

KNL is the FDA product code for Board, Scooter, Prone, a class I device type, regulated under 21 CFR 890.5370. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KNL
Device name
Board, Scooter, Prone
Regulation
21 CFR 890.5370
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
5
Ingested recalls
0

Clearances, product code KNL

By decision year
5 clearances under product code KNL with a decision year between 1978 and 1984, 1978 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code KNL by decision year
YearClearances
19782
19791
19811
19841

Applicants with the most clearances

Product code KNL
Applicants holding the most 510(k) clearances under product code KNL
ApplicantClearances
Fred Sammons, Inc.2
Maddak, Inc.2
Convaid Product Development1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 17 companies shown, in name order