Inofab Saglik Teknolojileri A.S is one of 37 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Inofab Saglik Teknolojileri A.S - FDA 510(k) Cleared Devices
Recent clearances: SpiroHome Personal, SpiroHome Clinic
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.
FDA 510(k) Regulatory Record - Inofab Saglik Teknolojileri A.S
1 devices