FDA 510(k)

PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS

K-Number: K020779 · 2002-06-05

Decision Date2002-06-05

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS 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 2002-06-05 under 510(k) number K020779. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS?

PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS is a medical device that received FDA 510(k) clearance on 2002-06-05. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K020779.

When did PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS receive FDA 510(k) clearance?

PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS received FDA 510(k) clearance on 2002-06-05, under 510(k) number K020779.

Who is the listed applicant for PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS?

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 PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS?

The FDA product code for PROXIMATE AND ENDOPATH LINEAR CUTTERS AND STAPLERS is GDW.

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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.