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FDA 510(k)

ANEURYSM CLIPS

K-Number: K013136 · 2001-11-26

ApplicantGistlstrasse
Decision Date2001-11-26
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANEURYSM CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Gistlstrasse. It received FDA 510(k) clearance on 2001-11-26 under 510(k) number K013136. 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 ANEURYSM CLIPS?

ANEURYSM CLIPS is a medical device that received FDA 510(k) clearance on 2001-11-26. The listed applicant is Gistlstrasse. The 510(k) number is K013136.

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

ANEURYSM CLIPS received FDA 510(k) clearance on 2001-11-26, under 510(k) number K013136.

Who is the listed applicant for ANEURYSM CLIPS?

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

What is the FDA product code for ANEURYSM CLIPS?

The FDA product code for 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.

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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