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FDA 510(k)

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

K-Number: K934174 · 1994-03-09

ApplicantETHICON, Inc.
Decision Date1994-03-09
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K934174. 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 LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER?

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is ETHICON, Inc.. The 510(k) number is K934174.

When did LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER receive FDA 510(k) clearance?

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER received FDA 510(k) clearance on 1994-03-09, under 510(k) number K934174.

Who is the listed applicant for LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER?

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 LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER?

The FDA product code for LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER is OCW.

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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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