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

Bed, Flotation Therapy, Powered

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

IOQ is the FDA product code for Bed, Flotation Therapy, Powered, a class II device type, regulated under 21 CFR 890.5170. As of , FDA records hold 57 510(k) clearances under this code, the most recent dated , and 35 recalls.

Classification record

Product code
IOQ
Device name
Bed, Flotation Therapy, Powered
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
57
Ingested recalls
38

Clearances, product code IOQ

By decision year
57 clearances under product code IOQ with a decision year between 1977 and 2015, 1988 the highest year at 7.
Show the numbers
510(k) clearances under FDA product code IOQ by decision year
YearClearances
19771
19831
19843
19862
19872
19887
19896
19906
19915
19925
19936
19941
19954
19975
19981
20131
20151

Applicants with the most clearances

Product code IOQ
Applicants holding the most 510(k) clearances under product code IOQ
ApplicantClearances
Hill-Rom Inc.7
KCI USA, Inc.5
Bio Clinic Co.4
Support Systems Intl.4
Gsi Development Co.3
Apex Metal, Inc.2
Dermanetics Corp.2
Medical Flotation Systems, Inc.2
Medical Group2
Western Medical, Ltd.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order