FDA 510(k)

VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR

K-Number: K051644 · 2005-08-11

Decision Date2005-08-11

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab. It received FDA 510(k) clearance on 2005-08-11 under 510(k) number K051644. 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 FORCETRIAD ELECTROSURGICAL GENERATOR?

VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2005-08-11. The listed applicant is Valleylab. The 510(k) number is K051644.

When did VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2005-08-11, under 510(k) number K051644.

Who is the listed applicant for VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR?

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 FORCETRIAD ELECTROSURGICAL GENERATOR?

The FDA product code for VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR 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.