FDA 510(k)

VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR

K-Number: K955035 · 1995-11-29

Decision Date1995-11-29

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Vidamed, Inc.. It received FDA 510(k) clearance on 1995-11-29 under 510(k) number K955035. 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 VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR?

VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1995-11-29. The listed applicant is Vidamed, Inc.. The 510(k) number is K955035.

When did VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1995-11-29, under 510(k) number K955035.

Who is the listed applicant for VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR?

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

What is the FDA product code for VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR?

The FDA product code for VIDAMED SERIES 7205 ELECTROSURGICAL 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.