FDA 510(k)

ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION

K-Number: K961264 · 1996-07-19

Decision Date1996-07-19

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 1996-07-19 under 510(k) number K961264. 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 ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION?

ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION is a medical device that received FDA 510(k) clearance on 1996-07-19. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K961264.

When did ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION receive FDA 510(k) clearance?

ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION received FDA 510(k) clearance on 1996-07-19, under 510(k) number K961264.

Who is the listed applicant for ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION?

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

What is the FDA product code for ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION?

The FDA product code for ENDOPATH EZ-RF LINEAR CUTTER AND COAGULATION is GEI.

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Other records listing Ethicon Endo-Surgery, Inc. as applicant

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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.