Cry IQ AB is one of 126 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Cry IQ AB - FDA 510(k) Cleared Devices
Recent clearances: CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED
1
Total
1
Cleared
0
Denied
Cry IQ AB has 1 FDA 510(k) cleared medical devices. Based in Onsala, SE.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cry IQ AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cry IQ AB
1 devices