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FDA 510(k)

MICROTYNE UNIT

K-Number: K760913 · 1976-11-12

Decision Date1976-11-12
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROTYNE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Transmed, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760913. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTYNE UNIT?

MICROTYNE UNIT is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Transmed, Inc.. The 510(k) number is K760913.

When did MICROTYNE UNIT receive FDA 510(k) clearance?

MICROTYNE UNIT received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760913.

Who is the listed applicant for MICROTYNE UNIT?

The FDA 510(k) record lists Transmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROTYNE UNIT?

The FDA product code for MICROTYNE UNIT is IPF.

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.

Other records listing Transmed, Inc. 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.

Related Devices (Code: IPF)

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.

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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