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FDA 510(k)

VANTAGECATH INTRAVASCULAR CATHETER

K-Number: K073471 · 2008-04-30

Decision Date2008-04-30
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VANTAGECATH INTRAVASCULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Device. It received FDA 510(k) clearance on 2008-04-30 under 510(k) number K073471. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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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