Inofab Saglik Teknolojileri A.S - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Inofab Saglik Teknolojileri A.S has 1 FDA 510(k) cleared medical devices. Based in Cankaya, Ankara, TR.
Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Inofab Saglik Teknolojileri A.S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Arazy Group Consultants, Inc. as regulatory consultant.
1 devices