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FDA 510(k)

GENERATOR, ELECTROSURGICAL

K-Number: K780206 · 1978-02-21

ApplicantValleylab, Inc.
Decision Date1978-02-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GENERATOR, ELECTROSURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780206. 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 GENERATOR, ELECTROSURGICAL?

GENERATOR, ELECTROSURGICAL is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Valleylab, Inc.. The 510(k) number is K780206.

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

GENERATOR, ELECTROSURGICAL received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780206.

Who is the listed applicant for GENERATOR, ELECTROSURGICAL?

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

What is the FDA product code for GENERATOR, ELECTROSURGICAL?

The FDA product code for GENERATOR, ELECTROSURGICAL 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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