FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

iCare ALTIUS CW

K Number: K234076 · Decision Aug 22, 2024
Classifications
1
FEI Numbers
31
Registration Numbers
32
Same Product Code
51
Applicant Total
13
Review Days
245

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
iCare ALTIUS CW
K Number
K234076
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Centervue S.P.A.
Date Received
December 21, 2023
Decision Date
August 22, 2024
Product Code
NFJ
Advisory Committee
Radiology
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NFJ System, Image Management, Ophthalmic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NFJ), ordered by most recent decision date.

View all

Other Clearances by Centervue S.P.A.

K Number Device Name
K243504 MAIA (AHMACME001)
K213705 DRSplus
K211328 EIDON FA, EIDON, EIDON AF, EIDON UWFL
K192113 DRSplus
K180526 EIDON FA
K180293 Retia 2
K153181 MAIA
K150320 COMPASS
K142047 EIDON
K133758 CENTERVUE MACULAR INTEGRITY ASSESSMENT
Search all 13 clearances from Centervue S.P.A. →