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FDA 510(k)

DEBUTRON

K-Number: K782119 · 1979-02-26

ApplicantMartin Electric Co.
Decision Date1979-02-26
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEBUTRON is the device name listed in this FDA 510(k) record. The listed applicant is Martin Electric Co.. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K782119. The device is classified under product code KCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEBUTRON?

DEBUTRON is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Martin Electric Co.. The 510(k) number is K782119.

When did DEBUTRON receive FDA 510(k) clearance?

DEBUTRON received FDA 510(k) clearance on 1979-02-26, under 510(k) number K782119.

Who is the listed applicant for DEBUTRON?

The FDA 510(k) record lists Martin Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEBUTRON?

The FDA product code for DEBUTRON is KCX.

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Related Devices (Code: KCX)

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.

K973773DAPELLE HAIR REMOVERWellquest Intl., Inc.K973340TWEEZER-TYPE EPILATORMobit, Inc.K973179FEMINIQUE SONIC HAIR REMOVERGlobal TV Concepts, Ltd.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K972695FINALLY FREEMehl/Group MarketingK970338TWEEZER-TYPE EPILATORIgia Direct, Inc.

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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