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

Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat

21 CFR 890.5275 / Physical Medicine
FDA source (opens on fda.gov)

IOA is the FDA product code for Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat, a class II device type, regulated under 21 CFR 890.5275. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IOA
Device name
Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat
Regulation
21 CFR 890.5275
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code IOA

By decision year
4 clearances under product code IOA with a decision year between 1986 and 1996, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IOA by decision year
YearClearances
19862
19901
19961

Applicants with the most clearances

Product code IOA
Applicants holding the most 510(k) clearances under product code IOA
ApplicantClearances
Cheung Laboratories, Inc.1
Elmed, Inc.1
Medical Microwave Research Corp.1
Nemectron Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code IOA.