Cimpax Aps is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Cimpax Aps - FDA 510(k) Cleared Devices
Recent clearances: C-CAT Anaesthesia Catheter kit
1
Total
1
Cleared
0
Denied
Cimpax Aps has 1 FDA 510(k) cleared medical devices. Based in Slangerup, DK.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Cimpax Aps Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Approvals, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cimpax Aps
1 devices