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FDA 510(k)

MAGNATHERM 2000

K-Number: K771540 · 1977-10-04

ApplicantIntl. Medical Electronics , Ltd.
Decision Date1977-10-04
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MAGNATHERM 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Electronics , Ltd.. It received FDA 510(k) clearance on 1977-10-04 under 510(k) number K771540. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNATHERM 2000?

MAGNATHERM 2000 is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is Intl. Medical Electronics , Ltd.. The 510(k) number is K771540.

When did MAGNATHERM 2000 receive FDA 510(k) clearance?

MAGNATHERM 2000 received FDA 510(k) clearance on 1977-10-04, under 510(k) number K771540.

Who is the listed applicant for MAGNATHERM 2000?

The FDA 510(k) record lists Intl. Medical Electronics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNATHERM 2000?

The FDA product code for MAGNATHERM 2000 is IMJ.

Related Clinical Trials

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.

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Other records listing Intl. Medical Electronics , Ltd. 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.

K934151MAGNATHERM MODEL 1000 SS

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

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

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