FDA 510(k)

CADD® Infusion Disposables Portfolio with NRFit connectors

K-Number: K162219 · 2017-07-20

Decision Date2017-07-20

Product CodePWH

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CADD® Infusion Disposables Portfolio with NRFit connectors is a medical device manufactured by Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2017-07-20 under approval number K162219. The device is classified under product code PWH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADD® Infusion Disposables Portfolio with NRFit connectors?

CADD® Infusion Disposables Portfolio with NRFit connectors is a medical device that received FDA 510(k) clearance on 2017-07-20. It is manufactured by Smiths Medical Asd, Inc.. The 510(k) number is K162219.

When was CADD® Infusion Disposables Portfolio with NRFit connectors approved by the FDA?

CADD® Infusion Disposables Portfolio with NRFit connectors received FDA 510(k) clearance on 2017-07-20, under approval number K162219.

What company makes CADD® Infusion Disposables Portfolio with NRFit connectors?

CADD® Infusion Disposables Portfolio with NRFit connectors is manufactured by Smiths Medical Asd, Inc..

What is the FDA product code for CADD® Infusion Disposables Portfolio with NRFit connectors?

The FDA product code for CADD® Infusion Disposables Portfolio with NRFit connectors is PWH.

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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.