Interfit A.G. Dba/Int'L Tanning Sys is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Interfit A.G. Dba/Int'L Tanning Sys - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Interfit A.G. Dba/Int'L Tanning Sys has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1984 to 1984. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Interfit A.G. Dba/Int'L Tanning Sys Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Interfit A.G. Dba/Int'L Tanning Sys
1 devices