510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860082Substantially Equivalent

Thermotron 918

Medical Microwave Research Corp., Silver Spring MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860082 is the FDA 510(k) clearance record for THERMOTRON 918, a class II device, cleared for Medical Microwave Research Corp. on under FDA product code IOA (Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat). FDA records list one 510(k) clearance for Medical Microwave Research Corp. As of , FDA records show no recalls naming K860082.

Clearance record

Decision date
Received
(78 days to decision)
Product code
IOA Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat
Regulation
21 CFR 890.5275
Device class
Class II
Review panel
Physical Medicine
Applicant
Medical Microwave Research Corp. 808 Pershing Dr. Suite 104, Silver Spring MD
Third party review
No

Clearances, product code IOA

Trailing 12 months

FDA records hold no clearances under product code IOA in the trailing twelve months.

FDA records show no clearances under product code IOA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IOA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260