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FDA 510(k)

WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER

K-Number: K021808 · 2002-08-14

ApplicantWeck
Decision Date2002-08-14
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Weck. It received FDA 510(k) clearance on 2002-08-14 under 510(k) number K021808. 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 WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER?

WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER is a medical device that received FDA 510(k) clearance on 2002-08-14. The listed applicant is Weck. The 510(k) number is K021808.

When did WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER receive FDA 510(k) clearance?

WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER received FDA 510(k) clearance on 2002-08-14, under 510(k) number K021808.

Who is the listed applicant for WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER?

The FDA 510(k) record lists Weck as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER?

The FDA product code for WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER is FZP.

Related Clinical Trials

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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Other records listing Weck as applicant

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.

K030311HEM-O-LOK XL CLIP

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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