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FDA 510(k)

RADAR VASCULAR COMPRESSION DEVICES

K-Number: K092503 · 2009-11-19

Decision Date2009-11-19
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RADAR VASCULAR COMPRESSION DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Vascular Dynamics. It received FDA 510(k) clearance on 2009-11-19 under 510(k) number K092503. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADAR VASCULAR COMPRESSION DEVICES?

RADAR VASCULAR COMPRESSION DEVICES is a medical device that received FDA 510(k) clearance on 2009-11-19. The listed applicant is Advanced Vascular Dynamics. The 510(k) number is K092503.

When did RADAR VASCULAR COMPRESSION DEVICES receive FDA 510(k) clearance?

RADAR VASCULAR COMPRESSION DEVICES received FDA 510(k) clearance on 2009-11-19, under 510(k) number K092503.

Who is the listed applicant for RADAR VASCULAR COMPRESSION DEVICES?

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

What is the FDA product code for RADAR VASCULAR COMPRESSION DEVICES?

The FDA product code for RADAR VASCULAR COMPRESSION DEVICES is DXC.

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 Advanced Vascular Dynamics 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: DXC)

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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