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FDA 510(k)

THERMO SHORTWAVE DIATHERMY

K-Number: K852166 · 1985-09-30

ApplicantZimmer Elektromedizin GmbH
Decision Date1985-09-30
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

THERMO SHORTWAVE DIATHERMY is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Elektromedizin GmbH. It received FDA 510(k) clearance on 1985-09-30 under 510(k) number K852166. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the THERMO SHORTWAVE DIATHERMY?

THERMO SHORTWAVE DIATHERMY is a medical device that received FDA 510(k) clearance on 1985-09-30. The listed applicant is Zimmer Elektromedizin GmbH. The 510(k) number is K852166.

When did THERMO SHORTWAVE DIATHERMY receive FDA 510(k) clearance?

THERMO SHORTWAVE DIATHERMY received FDA 510(k) clearance on 1985-09-30, under 510(k) number K852166.

Who is the listed applicant for THERMO SHORTWAVE DIATHERMY?

The FDA 510(k) record lists Zimmer Elektromedizin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMO SHORTWAVE DIATHERMY?

The FDA product code for THERMO SHORTWAVE DIATHERMY is IMJ.

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Other records listing Zimmer Elektromedizin GmbH as applicant

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.

K080735CRYOMINIK060395CRYO, MODEL V6.0K040727CRYO 5K960969GALVA 5-TK952536SONO 5K954411GALVA-5-M

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Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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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