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FDA 510(k)

EXPORT ASPIRATION CATHETER

K-Number: K023303 · 2002-10-29

Decision Date2002-10-29
Product CodeNFA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EXPORT ASPIRATION 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 2002-10-29 under 510(k) number K023303. The device is classified under product code NFA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPORT ASPIRATION CATHETER?

EXPORT ASPIRATION CATHETER is a medical device that received FDA 510(k) clearance on 2002-10-29. The listed applicant is Medtronic Vascular. The 510(k) number is K023303.

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

EXPORT ASPIRATION CATHETER received FDA 510(k) clearance on 2002-10-29, under 510(k) number K023303.

Who is the listed applicant for EXPORT ASPIRATION 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 EXPORT ASPIRATION CATHETER?

The FDA product code for EXPORT ASPIRATION CATHETER is NFA.

Related Clinical Trials

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.

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.

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Related Devices (Code: NFA)

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.

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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