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FDA 510(k)

OCCLUSION CLIPS

K-Number: K760961 · 1976-11-12

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-12
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

OCCLUSION CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760961. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCCLUSION CLIPS?

OCCLUSION CLIPS is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K760961.

When did OCCLUSION CLIPS receive FDA 510(k) clearance?

OCCLUSION CLIPS received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760961.

Who is the listed applicant for OCCLUSION CLIPS?

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

What is the FDA product code for OCCLUSION CLIPS?

The FDA product code for OCCLUSION CLIPS is HCH.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: HCH)

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.

K211183Sugita AVM MicroclipsMizuho America, Inc.K180757D-Clip; D-Clip ApplierPeter Lazic GmbHK091921CODMAN ANEURYSM CLIPS, CODMAN AVM MICRO CLIP SYSTEM, CODMAN SLIM-LINE GRAFT, REINFORCING, MINI ANEURYSM CLIPCodman & Shurtleff, Inc.K081640GIMMI ANEURYSM CLIPS AND APPLYING FORCEPSGimmi GmbHK081489L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERSPeter Lazic GmbHK060915KIRWAN L-ANEURYSM CLIPS AND APPLIER, KIRWAN YASARGIL-TYPE ANEURYSM CLIPS AND APPLIERSKirwan Surgical Products, Inc.

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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