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FDA 510(k)

ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH

K-Number: K031211 · 2003-07-17

ApplicantMedtronic Vascular
Decision Date2003-07-17
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2003-07-17 under 510(k) number K031211. 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 ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH?

ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Medtronic Vascular. The 510(k) number is K031211.

When did ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH receive FDA 510(k) clearance?

ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH received FDA 510(k) clearance on 2003-07-17, under 510(k) number K031211.

Who is the listed applicant for ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH?

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 ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH?

The FDA product code for ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH is DQY.

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Related Devices (Code: 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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