FDA 510(k)

ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106

K-Number: K024069 · 2003-01-08

Decision Date2003-01-08

Product CodeDWF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2003-01-08 under 510(k) number K024069. 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 ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106?

ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106 is a medical device that received FDA 510(k) clearance on 2003-01-08. The listed applicant is Medtronic Vascular. The 510(k) number is K024069.

When did ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106 receive FDA 510(k) clearance?

ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106 received FDA 510(k) clearance on 2003-01-08, under 510(k) number K024069.

Who is the listed applicant for ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106?

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 ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106?

The FDA product code for ONE PIECE PEDIATRIC ARTERIAL CANNULA, MODEL: 77006, 77106 is DWF.

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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.