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FDA 510(k)

AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP

K-Number: K032198 · 2003-08-20

ApplicantAesculap, Inc.
Decision Date2003-08-20
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2003-08-20 under 510(k) number K032198. 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 YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP?

AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP is a medical device that received FDA 510(k) clearance on 2003-08-20. The listed applicant is Aesculap, Inc.. The 510(k) number is K032198.

When did AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP receive FDA 510(k) clearance?

AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP received FDA 510(k) clearance on 2003-08-20, under 510(k) number K032198.

Who is the listed applicant for AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP?

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 YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP?

The FDA product code for AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP 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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