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FDA 510(k)

VIDAMED RF GENERATOR DATA RECORDER

K-Number: K963180 · 1996-10-10

ApplicantVidamed, Inc.
Decision Date1996-10-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIDAMED RF GENERATOR DATA RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Vidamed, Inc.. It received FDA 510(k) clearance on 1996-10-10 under 510(k) number K963180. 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 RF GENERATOR DATA RECORDER?

VIDAMED RF GENERATOR DATA RECORDER is a medical device that received FDA 510(k) clearance on 1996-10-10. The listed applicant is Vidamed, Inc.. The 510(k) number is K963180.

When did VIDAMED RF GENERATOR DATA RECORDER receive FDA 510(k) clearance?

VIDAMED RF GENERATOR DATA RECORDER received FDA 510(k) clearance on 1996-10-10, under 510(k) number K963180.

Who is the listed applicant for VIDAMED RF GENERATOR DATA RECORDER?

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 RF GENERATOR DATA RECORDER?

The FDA product code for VIDAMED RF GENERATOR DATA RECORDER is GEI.

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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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