VANTAGECATH INTRAVASCULAR CATHETER
K-Number: K073471 · 2008-04-30
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Device Summary
Frequently Asked Questions
What is the VANTAGECATH INTRAVASCULAR CATHETER?
VANTAGECATH INTRAVASCULAR CATHETER is a medical device that received FDA 510(k) clearance on 2008-04-30. The listed applicant is Advantage Medical Device. The 510(k) number is K073471.
When did VANTAGECATH INTRAVASCULAR CATHETER receive FDA 510(k) clearance?
VANTAGECATH INTRAVASCULAR CATHETER received FDA 510(k) clearance on 2008-04-30, under 510(k) number K073471.
Who is the listed applicant for VANTAGECATH INTRAVASCULAR CATHETER?
The FDA 510(k) record lists Advantage Medical Device as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VANTAGECATH INTRAVASCULAR CATHETER?
The FDA product code for VANTAGECATH INTRAVASCULAR CATHETER is FOZ.
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: FOZ)
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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