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FDA 510(k)

PROLENE POLYPROPYLENE LIGATING CLIP

K-Number: K811935 · 1981-09-11

ApplicantETHICON, Inc.
Decision Date1981-09-11
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROLENE POLYPROPYLENE 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 1981-09-11 under 510(k) number K811935. 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 PROLENE POLYPROPYLENE LIGATING CLIP?

PROLENE POLYPROPYLENE LIGATING CLIP is a medical device that received FDA 510(k) clearance on 1981-09-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K811935.

When did PROLENE POLYPROPYLENE LIGATING CLIP receive FDA 510(k) clearance?

PROLENE POLYPROPYLENE LIGATING CLIP received FDA 510(k) clearance on 1981-09-11, under 510(k) number K811935.

Who is the listed applicant for PROLENE POLYPROPYLENE 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 PROLENE POLYPROPYLENE LIGATING CLIP?

The FDA product code for PROLENE POLYPROPYLENE 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.

K260677Vessel Closure Device (VCD177213P)Vcd Medical S.R.L.K254231Inno-Hook™ Disposable Clip Appliers (Ligating Clips) and Inno-Hook™ Ligating ClipsTaiwan Surgical CorporationK253781InnoClip Clip ApplierTaiwan Surgical CorporationK253903InnoClip Disposable Clip ApplierTaiwan Surgical CorporationK250643Disposable Polymer Ligation ClipsHangzhou Kangji Medical Instrument Co., Ltd.K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsTeleflex Medical

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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