TAKA ANEURYSM CLIP
K-Number: K972750 · 1998-07-09
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Device Summary
Frequently Asked Questions
What is the TAKA ANEURYSM CLIP?
TAKA ANEURYSM CLIP is a medical device that received FDA 510(k) clearance on 1998-07-09. The listed applicant is V. Mueller Neuro/Spine. The 510(k) number is K972750.
When did TAKA ANEURYSM CLIP receive FDA 510(k) clearance?
TAKA ANEURYSM CLIP received FDA 510(k) clearance on 1998-07-09, under 510(k) number K972750.
Who is the listed applicant for TAKA ANEURYSM CLIP?
The FDA 510(k) record lists V. Mueller Neuro/Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAKA ANEURYSM CLIP?
The FDA product code for TAKA 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 V. Mueller Neuro/Spine 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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