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FDA 510(k)

ETHICON ARTHROSCOPIC KNOT PUSHER

K-Number: K952814 · 1995-07-11

ApplicantETHICON, Inc.
Decision Date1995-07-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ETHICON ARTHROSCOPIC 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 1995-07-11 under 510(k) number K952814. 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 ETHICON ARTHROSCOPIC KNOT PUSHER?

ETHICON ARTHROSCOPIC KNOT PUSHER is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K952814.

When did ETHICON ARTHROSCOPIC KNOT PUSHER receive FDA 510(k) clearance?

ETHICON ARTHROSCOPIC KNOT PUSHER received FDA 510(k) clearance on 1995-07-11, under 510(k) number K952814.

Who is the listed applicant for ETHICON ARTHROSCOPIC 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 ETHICON ARTHROSCOPIC KNOT PUSHER?

The FDA product code for ETHICON ARTHROSCOPIC KNOT PUSHER is GCJ.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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