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FDA 510(k)

LIGACLIP 20/20* MULTIPLE CLIP APPLIER

K-Number: K864102 · 1986-11-05

ApplicantETHICON, Inc.
Decision Date1986-11-05
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGACLIP 20/20* 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 1986-11-05 under 510(k) number K864102. 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 20/20* MULTIPLE CLIP APPLIER?

LIGACLIP 20/20* MULTIPLE CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1986-11-05. The listed applicant is ETHICON, Inc.. The 510(k) number is K864102.

When did LIGACLIP 20/20* MULTIPLE CLIP APPLIER receive FDA 510(k) clearance?

LIGACLIP 20/20* MULTIPLE CLIP APPLIER received FDA 510(k) clearance on 1986-11-05, under 510(k) number K864102.

Who is the listed applicant for LIGACLIP 20/20* 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 20/20* MULTIPLE CLIP APPLIER?

The FDA product code for LIGACLIP 20/20* 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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