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

Components, Exercise

21 CFR 890.5350 / Physical Medicine
FDA source (opens on fda.gov)

IOD is the FDA product code for Components, Exercise, a class I device type, regulated under 21 CFR 890.5350. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IOD
Device name
Components, Exercise
Regulation
21 CFR 890.5350
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
11
Ingested recalls
0

Clearances, product code IOD

By decision year
11 clearances under product code IOD with a decision year between 1976 and 1983, 1983 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code IOD by decision year
YearClearances
19762
19771
19781
19791
19811
19822
19833

Applicants with the most clearances

Product code IOD
Applicants holding the most 510(k) clearances under product code IOD
ApplicantClearances
Fred Sammons, Inc.7
Danek Medical, Inc.1
Kaye Products, Inc.1
Maddak, Inc.1
Stat Medical Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 106 companies shown, in name order