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FDA 510(k)

MADTRONIC DLP ARTERIAL CANNULAE

K-Number: K991066 · 1999-09-14

ApplicantMedtronic Vascular
Decision Date1999-09-14
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MADTRONIC DLP ARTERIAL CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1999-09-14 under 510(k) number K991066. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MADTRONIC DLP ARTERIAL CANNULAE?

MADTRONIC DLP ARTERIAL CANNULAE is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Medtronic Vascular. The 510(k) number is K991066.

When did MADTRONIC DLP ARTERIAL CANNULAE receive FDA 510(k) clearance?

MADTRONIC DLP ARTERIAL CANNULAE received FDA 510(k) clearance on 1999-09-14, under 510(k) number K991066.

Who is the listed applicant for MADTRONIC DLP ARTERIAL CANNULAE?

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 MADTRONIC DLP ARTERIAL CANNULAE?

The FDA product code for MADTRONIC DLP ARTERIAL CANNULAE is DWF.

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Other records listing Medtronic Vascular as applicant

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Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, 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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