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FDA 510(k)

Medtronic Bio-Medicus Adult Cannula Kit

K-Number: K153598 · 2016-01-15

ApplicantMedtronic, Inc.
Decision Date2016-01-15
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medtronic Bio-Medicus Adult Cannula Kit is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2016-01-15 under approval number K153598. 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 Medtronic Bio-Medicus Adult Cannula Kit?

Medtronic Bio-Medicus Adult Cannula Kit is a medical device that received FDA 510(k) clearance on 2016-01-15. It is manufactured by Medtronic, Inc.. The 510(k) number is K153598.

When was Medtronic Bio-Medicus Adult Cannula Kit approved by the FDA?

Medtronic Bio-Medicus Adult Cannula Kit received FDA 510(k) clearance on 2016-01-15, under approval number K153598.

What company makes Medtronic Bio-Medicus Adult Cannula Kit?

Medtronic Bio-Medicus Adult Cannula Kit is manufactured by Medtronic, Inc..

What is the FDA product code for Medtronic Bio-Medicus Adult Cannula Kit?

The FDA product code for Medtronic Bio-Medicus Adult Cannula Kit is DWF.

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Related Devices (Code: 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.

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