CADD® Infusion Disposables Portfolio with NRFit™ connectors
K-Number: K162219 · 2017-07-20
Device Summary
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. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K162219.
When did CADD® Infusion Disposables Portfolio with NRFit™ connectors receive FDA 510(k) clearance?
CADD® Infusion Disposables Portfolio with NRFit™ connectors received FDA 510(k) clearance on 2017-07-20, under 510(k) number K162219.
Who is the listed applicant for CADD® Infusion Disposables Portfolio with NRFit™ connectors?
The FDA 510(k) record lists Smiths Medical Asd, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Smiths Medical Asd, Inc. as applicant
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.
Related Devices (Code: PWH)
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.
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.