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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 the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2019-09-20 under 510(k) 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. The listed applicant is Medtronic Vascular. The 510(k) number is K192296.

When did Medtronic 6F Taiga Guiding Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Medtronic 6F Taiga Guiding Catheter?

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 6F Taiga Guiding Catheter?

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

Related Clinical Trials

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Other records listing Medtronic Vascular 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.

PMA P160043Coronary drug-eluting stentPMA P110023STENT, SUPERFICIAL FEMORAL ARTERYPMA P060001Stent, carotidPMA P190008Drug-coated peripheral transluminal angioplasty catheterPMA P100021SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENTPMA P200026Stent, iliac vein

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Related Devices (Code: DQY)

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.

K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbottK261631Amplatzer TorqVue Exchange SystemAbbott Medical

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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