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

Cushion, Flotation, Therapeutic

21 CFR 890.5170 / Physical Medicine
FDA source (opens on fda.gov)

MOC is the FDA product code for Cushion, Flotation, Therapeutic, a class II device type, regulated under 21 CFR 890.5170. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MOC
Device name
Cushion, Flotation, Therapeutic
Regulation
21 CFR 890.5170
Device class
Class II
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 MOC

By decision year
2 clearances under product code MOC with a decision year between 1995 and 2008, 1995 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MOC by decision year
YearClearances
19951
20081

Applicants with the most clearances

Product code MOC
Applicants holding the most 510(k) clearances under product code MOC
ApplicantClearances
Ergo-Air, Inc.1
Medical Technology Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code