Koninklijke (Royal) Utermohlen is one of 143 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Koninklijke (Royal) Utermohlen - FDA 510(k) Cleared Devices
Recent clearances: UTERMOHLEN CRYO PROFESSIONAL
1
Total
1
Cleared
0
Denied
Koninklijke (Royal) Utermohlen has 1 FDA 510(k) cleared medical devices. Based in Wolvega, NL.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Koninklijke (Royal) Utermohlen Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Krm Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Koninklijke (Royal) Utermohlen
1 devices