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FDA 510(k)

ENDOPATH DISPOSABLE KNOT PUSHER

K-Number: K931238 · 1993-06-22

ApplicantETHICON, Inc.
Decision Date1993-06-22
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH DISPOSABLE KNOT PUSHER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K931238. 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 KNOT PUSHER?

ENDOPATH DISPOSABLE KNOT PUSHER is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is ETHICON, Inc.. The 510(k) number is K931238.

When did ENDOPATH DISPOSABLE KNOT PUSHER receive FDA 510(k) clearance?

ENDOPATH DISPOSABLE KNOT PUSHER received FDA 510(k) clearance on 1993-06-22, under 510(k) number K931238.

Who is the listed applicant for ENDOPATH DISPOSABLE KNOT PUSHER?

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 KNOT PUSHER?

The FDA product code for ENDOPATH DISPOSABLE KNOT PUSHER is GCJ.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: 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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