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FDA 510(k)

DAVIS & GECK LIGATING CLIP REMOVER

K-Number: K953908 · 1995-11-30

ApplicantDavis & Geck, Inc.
Decision Date1995-11-30
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVIS & GECK LIGATING CLIP REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1995-11-30 under 510(k) number K953908. 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 DAVIS & GECK LIGATING CLIP REMOVER?

DAVIS & GECK LIGATING CLIP REMOVER is a medical device that received FDA 510(k) clearance on 1995-11-30. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K953908.

When did DAVIS & GECK LIGATING CLIP REMOVER receive FDA 510(k) clearance?

DAVIS & GECK LIGATING CLIP REMOVER received FDA 510(k) clearance on 1995-11-30, under 510(k) number K953908.

Who is the listed applicant for DAVIS & GECK LIGATING CLIP REMOVER?

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

What is the FDA product code for DAVIS & GECK LIGATING CLIP REMOVER?

The FDA product code for DAVIS & GECK LIGATING CLIP REMOVER is FZP.

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Other records listing Davis & Geck, Inc. as applicant

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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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