FDA 510(k)

ELECTROSURGICAL CUT AND COAGU ACCESSORY

K-Number: K791362 · 1979-09-04

Decision Date1979-09-04

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CUT AND COAGU ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1979-09-04 under 510(k) number K791362. 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 ELECTROSURGICAL CUT AND COAGU ACCESSORY?

ELECTROSURGICAL CUT AND COAGU ACCESSORY is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Intermedics, Inc.. The 510(k) number is K791362.

When did ELECTROSURGICAL CUT AND COAGU ACCESSORY receive FDA 510(k) clearance?

ELECTROSURGICAL CUT AND COAGU ACCESSORY received FDA 510(k) clearance on 1979-09-04, under 510(k) number K791362.

Who is the listed applicant for ELECTROSURGICAL CUT AND COAGU ACCESSORY?

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

What is the FDA product code for ELECTROSURGICAL CUT AND COAGU ACCESSORY?

The FDA product code for ELECTROSURGICAL CUT AND COAGU ACCESSORY is GEI.

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Official Source

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