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FDA 510(k)

VIDAMED MODEDL 7600 RF GENERATOR

K-Number: K965061 · 1997-01-28

ApplicantVidamed, Inc.
Decision Date1997-01-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIDAMED MODEDL 7600 RF 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 1997-01-28 under 510(k) number K965061. 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 MODEDL 7600 RF GENERATOR?

VIDAMED MODEDL 7600 RF GENERATOR is a medical device that received FDA 510(k) clearance on 1997-01-28. The listed applicant is Vidamed, Inc.. The 510(k) number is K965061.

When did VIDAMED MODEDL 7600 RF GENERATOR receive FDA 510(k) clearance?

VIDAMED MODEDL 7600 RF GENERATOR received FDA 510(k) clearance on 1997-01-28, under 510(k) number K965061.

Who is the listed applicant for VIDAMED MODEDL 7600 RF 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 MODEDL 7600 RF GENERATOR?

The FDA product code for VIDAMED MODEDL 7600 RF GENERATOR is GEI.

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Other records listing Vidamed, Inc. as applicant

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Official Source

View on FDA Database →

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

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