Roger Cestac & Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Roger Cestac & Assoc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Roger Cestac & Assoc. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1981 to 1981. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Roger Cestac & Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Roger Cestac & Assoc.
2 devices