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FDA 510(k)

VASORING* VRC VASCULAR RING CONNECTOR

K-Number: K061626 · 2006-10-05

Decision Date2006-10-05
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASORING* VRC VASCULAR RING CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Sunwei Tech Co. , Ltd.. It received FDA 510(k) clearance on 2006-10-05 under 510(k) number K061626. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASORING* VRC VASCULAR RING CONNECTOR?

VASORING* VRC VASCULAR RING CONNECTOR is a medical device that received FDA 510(k) clearance on 2006-10-05. The listed applicant is Sunwei Tech Co. , Ltd.. The 510(k) number is K061626.

When did VASORING* VRC VASCULAR RING CONNECTOR receive FDA 510(k) clearance?

VASORING* VRC VASCULAR RING CONNECTOR received FDA 510(k) clearance on 2006-10-05, under 510(k) number K061626.

Who is the listed applicant for VASORING* VRC VASCULAR RING CONNECTOR?

The FDA 510(k) record lists Sunwei Tech Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASORING* VRC VASCULAR RING CONNECTOR?

The FDA product code for VASORING* VRC VASCULAR RING CONNECTOR is DSY.

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: DSY)

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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