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FDA 510(k)

ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN

K-Number: K915099 · 1992-03-19

ApplicantETHICON, Inc.
Decision Date1992-03-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1992-03-19 under 510(k) number K915099. 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 ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN?

ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN is a medical device that received FDA 510(k) clearance on 1992-03-19. The listed applicant is ETHICON, Inc.. The 510(k) number is K915099.

When did ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN receive FDA 510(k) clearance?

ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN received FDA 510(k) clearance on 1992-03-19, under 510(k) number K915099.

Who is the listed applicant for ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN?

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 ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN?

The FDA product code for ENDOPATH ENDOS LINEAR CUT W/SAF LOCK-OUT/RELOAD UN is 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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