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FDA 510(k)

THERMOTRON 918

K-Number: K860082 · 1986-03-27

ApplicantMedical Microwave Research Corp.
Decision Date1986-03-27
Product CodeIOA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERMOTRON 918 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Microwave Research Corp.. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K860082. The device is classified under product code IOA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOTRON 918?

THERMOTRON 918 is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Medical Microwave Research Corp.. The 510(k) number is K860082.

When did THERMOTRON 918 receive FDA 510(k) clearance?

THERMOTRON 918 received FDA 510(k) clearance on 1986-03-27, under 510(k) number K860082.

Who is the listed applicant for THERMOTRON 918?

The FDA 510(k) record lists Medical Microwave Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMOTRON 918?

The FDA product code for THERMOTRON 918 is IOA.

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Related Devices (Code: IOA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K941567DIATHERMY DEVICE-MICROFOCUSCheung Laboratories, Inc.K895000NEMECTRON MICROWAVENemectron Medical, Inc.K862029SIEMENS RADIOTHERM 706, MICROWAVE THERAPY UNITElmed, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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