TEMPORARY TITANIUM ANEURYSM CLIP
K-Number: K031468 · 2003-06-20
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Device Summary
Frequently Asked Questions
What is the TEMPORARY TITANIUM ANEURYSM CLIP?
TEMPORARY TITANIUM ANEURYSM CLIP is a medical device that received FDA 510(k) clearance on 2003-06-20. The listed applicant is Cardinalhealth. The 510(k) number is K031468.
When did TEMPORARY TITANIUM ANEURYSM CLIP receive FDA 510(k) clearance?
TEMPORARY TITANIUM ANEURYSM CLIP received FDA 510(k) clearance on 2003-06-20, under 510(k) number K031468.
Who is the listed applicant for TEMPORARY TITANIUM ANEURYSM CLIP?
The FDA 510(k) record lists Cardinalhealth as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEMPORARY TITANIUM ANEURYSM CLIP?
The FDA product code for TEMPORARY TITANIUM ANEURYSM CLIP 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 Cardinalhealth 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.
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
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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