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FDA 510(k)

MEDICON TITANIUM YASARGIL ANEURYSM CLIPS

K-Number: K010908 · 2001-08-01

ApplicantMedicon EG
Decision Date2001-08-01
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDICON TITANIUM YASARGIL ANEURYSM CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Medicon EG. It received FDA 510(k) clearance on 2001-08-01 under 510(k) number K010908. 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 MEDICON TITANIUM YASARGIL ANEURYSM CLIPS?

MEDICON TITANIUM YASARGIL ANEURYSM CLIPS is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Medicon EG. The 510(k) number is K010908.

When did MEDICON TITANIUM YASARGIL ANEURYSM CLIPS receive FDA 510(k) clearance?

MEDICON TITANIUM YASARGIL ANEURYSM CLIPS received FDA 510(k) clearance on 2001-08-01, under 510(k) number K010908.

Who is the listed applicant for MEDICON TITANIUM YASARGIL ANEURYSM CLIPS?

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

What is the FDA product code for MEDICON TITANIUM YASARGIL ANEURYSM CLIPS?

The FDA product code for MEDICON TITANIUM YASARGIL ANEURYSM CLIPS is HCH.

Related Clinical Trials

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.

Other records listing Medicon EG 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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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