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FDA 510(k)

LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER

K-Number: K050344 · 2005-03-14

ApplicantEthicon Endo Surgery, Inc.
Decision Date2005-03-14
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER 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 2005-03-14 under 510(k) number K050344. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER?

LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER is a medical device that received FDA 510(k) clearance on 2005-03-14. The listed applicant is Ethicon Endo Surgery, Inc.. The 510(k) number is K050344.

When did LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER receive FDA 510(k) clearance?

LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER received FDA 510(k) clearance on 2005-03-14, under 510(k) number K050344.

Who is the listed applicant for LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER?

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 LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER?

The FDA product code for LIGACLIP 5 M/L MM ENDOSCOPIC MULTIPLE CLIP APPLIER is FZP.

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Related Devices (Code: FZP)

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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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