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

Belt, Wheelchair

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

IQB is the FDA product code for Belt, 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 no recalls.

Classification record

Product code
IQB
Device name
Belt, 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
0

Clearances, product code IQB

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

Applicants with the most clearances

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

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 56 companies shown, in name order