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FDA 510(k)

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER

K-Number: K904907 · 1991-01-24

ApplicantETHICON, Inc.
Decision Date1991-01-24
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1991-01-24 under 510(k) number K904907. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER?

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER is a medical device that received FDA 510(k) clearance on 1991-01-24. The listed applicant is ETHICON, Inc.. The 510(k) number is K904907.

When did ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER receive FDA 510(k) clearance?

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER received FDA 510(k) clearance on 1991-01-24, under 510(k) number K904907.

Who is the listed applicant for ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER?

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 SURGICAL TROCAR REDUCER?

The FDA product code for ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER is HET.

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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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