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

Board, Lap, Wheelchair

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

IMX is the FDA product code for Board, Lap, Wheelchair, a class I device type, regulated under 21 CFR 890.3910. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IMX
Device name
Board, Lap, 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
2
Ingested recalls
0

Clearances, product code IMX

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

Applicants with the most clearances

Product code IMX
Applicants holding the most 510(k) clearances under product code IMX
ApplicantClearances
Fred Sammons, Inc.1
Orthopedic Equipment Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 35 companies shown, in name order