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FDA 510(k)

MODIFIED ENDOPATH ILS

K-Number: K940967 · 1994-05-27

ApplicantEthicon Endo-Surgery, Inc.
Decision Date1994-05-27
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED ENDOPATH ILS 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 1994-05-27 under 510(k) number K940967. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ENDOPATH ILS?

MODIFIED ENDOPATH ILS is a medical device that received FDA 510(k) clearance on 1994-05-27. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K940967.

When did MODIFIED ENDOPATH ILS receive FDA 510(k) clearance?

MODIFIED ENDOPATH ILS received FDA 510(k) clearance on 1994-05-27, under 510(k) number K940967.

Who is the listed applicant for MODIFIED ENDOPATH ILS?

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 MODIFIED ENDOPATH ILS?

The FDA product code for MODIFIED ENDOPATH ILS is OCW.

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

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Related Devices (Code: OCW)

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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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