FDA 510(k)

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT

K-Number: K993677 · 2000-04-17

Decision Date2000-04-17

Product CodeDWF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2000-04-17 under 510(k) number K993677. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT?

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT is a medical device that received FDA 510(k) clearance on 2000-04-17. The listed applicant is Medtronic Vascular. The 510(k) number is K993677.

When did MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT receive FDA 510(k) clearance?

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT received FDA 510(k) clearance on 2000-04-17, under 510(k) number K993677.

Who is the listed applicant for MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT?

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

What is the FDA product code for MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT?

The FDA product code for MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT is DWF.

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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.