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FDA 510(k)

MEDTRONIC EXPORT XT CATHETER

K-Number: K061958 · 2006-09-05

ApplicantMedtronic Vascular
Decision Date2006-09-05
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC EXPORT XT 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 2006-09-05 under 510(k) number K061958. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC EXPORT XT CATHETER?

MEDTRONIC EXPORT XT CATHETER is a medical device that received FDA 510(k) clearance on 2006-09-05. The listed applicant is Medtronic Vascular. The 510(k) number is K061958.

When did MEDTRONIC EXPORT XT CATHETER receive FDA 510(k) clearance?

MEDTRONIC EXPORT XT CATHETER received FDA 510(k) clearance on 2006-09-05, under 510(k) number K061958.

Who is the listed applicant for MEDTRONIC EXPORT XT 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 EXPORT XT CATHETER?

The FDA product code for MEDTRONIC EXPORT XT CATHETER is QEZ.

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Other records listing Medtronic Vascular as applicant

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Related Devices (Code: QEZ)

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.

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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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