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FDA 510(k)

ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR

K-Number: K915239 · 1992-01-15

ApplicantETHICON, Inc.
Decision Date1992-01-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1992-01-15 under 510(k) number K915239. 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 DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR?

ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is ETHICON, Inc.. The 510(k) number is K915239.

When did ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR receive FDA 510(k) clearance?

ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR received FDA 510(k) clearance on 1992-01-15, under 510(k) number K915239.

Who is the listed applicant for ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR?

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 TROCAR SLEEVE W/DILATING OBTUR?

The FDA product code for ENDOPATH DISPOSABLE TROCAR SLEEVE W/DILATING OBTUR is GCJ.

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Related Devices (Code: GCJ)

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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.

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