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FDA 510(k)

AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200

K-Number: K851251 · 1985-07-02

ApplicantEdward Weck, Inc.
Decision Date1985-07-02
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851251. 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 AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200?

AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Edward Weck, Inc.. The 510(k) number is K851251.

When did AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 receive FDA 510(k) clearance?

AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851251.

Who is the listed applicant for AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200?

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

What is the FDA product code for AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200?

The FDA product code for AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 is FZP.

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Other records listing Edward Weck, Inc. 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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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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 CorporationK253903InnoClip Disposable Clip ApplierTaiwan Surgical CorporationK253781InnoClip 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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