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FDA 510(k)

LIGACLIP TITANIUM LIGATING CLIP

K-Number: K830503 · 1983-03-08

ApplicantETHICON, Inc.
Decision Date1983-03-08
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGACLIP TITANIUM LIGATING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1983-03-08 under 510(k) number K830503. 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 TITANIUM LIGATING CLIP?

LIGACLIP TITANIUM LIGATING CLIP is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is ETHICON, Inc.. The 510(k) number is K830503.

When did LIGACLIP TITANIUM LIGATING CLIP receive FDA 510(k) clearance?

LIGACLIP TITANIUM LIGATING CLIP received FDA 510(k) clearance on 1983-03-08, under 510(k) number K830503.

Who is the listed applicant for LIGACLIP TITANIUM LIGATING CLIP?

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 TITANIUM LIGATING CLIP?

The FDA product code for LIGACLIP TITANIUM LIGATING CLIP is FZP.

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Related Devices (Code: FZP)

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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