FDA 510(k)

PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES

K-Number: K991030 · 1999-05-17

Decision Date1999-05-17

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES 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 1999-05-17 under 510(k) number K991030. 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 HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES?

PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K991030.

When did PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES receive FDA 510(k) clearance?

PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES received FDA 510(k) clearance on 1999-05-17, under 510(k) number K991030.

Who is the listed applicant for PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES?

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 HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES?

The FDA product code for PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES is GDW.

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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.