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FDA 510(k)

AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)

K-Number: K043041 · 2004-12-09

ApplicantAesculap, Inc.
Decision Date2004-12-09
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX) is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2004-12-09 under 510(k) number K043041. 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 AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)?

AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX) is a medical device that received FDA 510(k) clearance on 2004-12-09. The listed applicant is Aesculap, Inc.. The 510(k) number is K043041.

When did AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX) receive FDA 510(k) clearance?

AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX) received FDA 510(k) clearance on 2004-12-09, under 510(k) number K043041.

Who is the listed applicant for AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)?

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

What is the FDA product code for AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)?

The FDA product code for AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX) is HCH.

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Other records listing Aesculap, 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.

K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

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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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