iCare ALTIUS CW
K-Number: K234076 · 2024-08-22
ApplicantCentervue S.P.A.
Decision Date2024-08-22
Product CodeNFJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
iCare ALTIUS CW is a medical device manufactured by Centervue S.P.A.. It received FDA 510(k) clearance on 2024-08-22 under approval number K234076. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the iCare ALTIUS CW?
iCare ALTIUS CW is a medical device that received FDA 510(k) clearance on 2024-08-22. It is manufactured by Centervue S.P.A.. The 510(k) number is K234076.
When was iCare ALTIUS CW approved by the FDA?
iCare ALTIUS CW received FDA 510(k) clearance on 2024-08-22, under approval number K234076.
What company makes iCare ALTIUS CW?
iCare ALTIUS CW is manufactured by Centervue S.P.A..
What is the FDA product code for iCare ALTIUS CW?
The FDA product code for iCare ALTIUS CW is NFJ.
Other Devices by Centervue S.P.A.
Related Devices (Code: NFJ)
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.