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FDA 510(k)

ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE

K-Number: K920110 · 1992-04-02

ApplicantETHICON, Inc.
Decision Date1992-04-02
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1992-04-02 under 510(k) number K920110. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE?

ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is ETHICON, Inc.. The 510(k) number is K920110.

When did ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE receive FDA 510(k) clearance?

ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE received FDA 510(k) clearance on 1992-04-02, under 510(k) number K920110.

Who is the listed applicant for ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE?

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

What is the FDA product code for ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE?

The FDA product code for ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE is GEA.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: GEA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, Inc.K904881DISPOSABLE YANKAUER SUCTION TUBEPilling Medical S.A.

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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