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FDA 510(k)

Medtronic 6F Taiga Guiding Catheter

K-Number: K192296 · 2019-09-20

ApplicantMedtronic Vascular
Decision Date2019-09-20
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medtronic 6F Taiga Guiding Catheter is a medical device manufactured by Medtronic Vascular. It received FDA 510(k) clearance on 2019-09-20 under approval number K192296. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medtronic 6F Taiga Guiding Catheter?

Medtronic 6F Taiga Guiding Catheter is a medical device that received FDA 510(k) clearance on 2019-09-20. It is manufactured by Medtronic Vascular. The 510(k) number is K192296.

When was Medtronic 6F Taiga Guiding Catheter approved by the FDA?

Medtronic 6F Taiga Guiding Catheter received FDA 510(k) clearance on 2019-09-20, under approval number K192296.

What company makes Medtronic 6F Taiga Guiding Catheter?

Medtronic 6F Taiga Guiding Catheter is manufactured by Medtronic Vascular.

What is the FDA product code for Medtronic 6F Taiga Guiding Catheter?

The FDA product code for Medtronic 6F Taiga Guiding Catheter is DQY.

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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.

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