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FDA 510(k)

MODEL 6400 ABC ELECTROSURGERY GENERATOR

K-Number: K933332 · 1993-09-23

ApplicantWilliam E. Mckay
Decision Date1993-09-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 6400 ABC ELECTROSURGERY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is William E. Mckay. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K933332. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6400 ABC ELECTROSURGERY GENERATOR?

MODEL 6400 ABC ELECTROSURGERY GENERATOR is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is William E. Mckay. The 510(k) number is K933332.

When did MODEL 6400 ABC ELECTROSURGERY GENERATOR receive FDA 510(k) clearance?

MODEL 6400 ABC ELECTROSURGERY GENERATOR received FDA 510(k) clearance on 1993-09-23, under 510(k) number K933332.

Who is the listed applicant for MODEL 6400 ABC ELECTROSURGERY GENERATOR?

The FDA 510(k) record lists William E. Mckay as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 6400 ABC ELECTROSURGERY GENERATOR?

The FDA product code for MODEL 6400 ABC ELECTROSURGERY GENERATOR is GEI.

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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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