Tulan Corp. C/O Richard Hamer Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tulan Corp. C/O Richard Hamer Assoc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tulan Corp. C/O Richard Hamer Assoc. has 2 FDA 510(k) cleared medical devices. Based in Sterling, US.
Historical record: 2 cleared submissions from 1988 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tulan Corp. C/O Richard Hamer Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tulan Corp. C/O Richard Hamer Assoc.
2 devices