FDA 510(k)

ENDOPATH ENDOSCOPIC INSTRUMENTS

K-Number: K984240 · 1999-06-22

Decision Date1999-06-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ENDOPATH ENDOSCOPIC INSTRUMENTS 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 1999-06-22 under 510(k) number K984240. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH ENDOSCOPIC INSTRUMENTS?

ENDOPATH ENDOSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1999-06-22. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K984240.

When did ENDOPATH ENDOSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

ENDOPATH ENDOSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1999-06-22, under 510(k) number K984240.

Who is the listed applicant for ENDOPATH ENDOSCOPIC INSTRUMENTS?

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 ENDOSCOPIC INSTRUMENTS?

The FDA product code for ENDOPATH ENDOSCOPIC INSTRUMENTS is GEI.

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

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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.