FDA 510(k)

VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT

K-Number: K051627 · 2005-07-22

Decision Date2005-07-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab. It received FDA 510(k) clearance on 2005-07-22 under 510(k) number K051627. 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 VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT?

VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 2005-07-22. The listed applicant is Valleylab. The 510(k) number is K051627.

When did VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT receive FDA 510(k) clearance?

VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT received FDA 510(k) clearance on 2005-07-22, under 510(k) number K051627.

Who is the listed applicant for VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT?

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

What is the FDA product code for VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT?

The FDA product code for VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT 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.