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FDA 510(k)

ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER

K-Number: K920847 · 1992-05-29

ApplicantETHICON, Inc.
Decision Date1992-05-29
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1992-05-29 under 510(k) number K920847. 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 ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER?

ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER is a medical device that received FDA 510(k) clearance on 1992-05-29. The listed applicant is ETHICON, Inc.. The 510(k) number is K920847.

When did ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER receive FDA 510(k) clearance?

ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER received FDA 510(k) clearance on 1992-05-29, under 510(k) number K920847.

Who is the listed applicant for ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER?

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 LIGACLIP ENDO LD APPLIER/DIVIDER?

The FDA product code for ETHICON LIGACLIP ENDO LD APPLIER/DIVIDER 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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