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FDA 510(k)

MODIFICATION TO EXPORT ASPIRATION CATHETER

K-Number: K030201 · 2003-03-26

ApplicantMedtronic Vascular
Decision Date2003-03-26
Product CodeNFA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO 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 2003-03-26 under 510(k) number K030201. 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 MODIFICATION TO EXPORT ASPIRATION CATHETER?

MODIFICATION TO EXPORT ASPIRATION CATHETER is a medical device that received FDA 510(k) clearance on 2003-03-26. The listed applicant is Medtronic Vascular. The 510(k) number is K030201.

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

MODIFICATION TO EXPORT ASPIRATION CATHETER received FDA 510(k) clearance on 2003-03-26, under 510(k) number K030201.

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

The FDA product code for MODIFICATION TO EXPORT ASPIRATION CATHETER is NFA.

Related Clinical Trials

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Other records listing Medtronic Vascular as applicant

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K232570Steerant™ Super Stiff GuidewireK2321906F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide CatheterK2301565F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide CatheterK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)K192296Medtronic 6F Taiga Guiding CatheterK173515Admiral Xtreme

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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.

K073523INTERCEPTOR PLUS CORONARY FILTER SYSTEMSMedtronic, Inc.K073563MODIFICATION TO PROXIS SYSTEMSt Jude MedicalK063785SPIDERFX EMBOLIC PROTECTION DEVICEEv3, Inc.K062870TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03Kensey Nash Corp.K060651PROXIS SYSTEM, MODEL EPS101St Jude MedicalK052523PROXIS SYSTEMVelocimed, Inc.

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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