Dayton Mfg. Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dayton Mfg. Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Dayton Mfg. Co. has 2 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 2 cleared submissions from 1987 to 1987. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Dayton Mfg. Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dayton Mfg. Co.
2 devices