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FDA 510(k)

ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE

K-Number: K952842 · 1995-07-31

ApplicantEthicon Endo-Surgery, Inc.
Decision Date1995-07-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE 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 1995-07-31 under 510(k) number K952842. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE?

ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K952842.

When did ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE receive FDA 510(k) clearance?

ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952842.

Who is the listed applicant for ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE?

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* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE?

The FDA product code for ENDOPATH* TRISTAR FLAT BLADED SURGICAL OBTURATOR & SLEEVE is GCJ.

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

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Related Devices (Code: GCJ)

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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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