Hyman, Phelps & McNamara, P.C. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hyman, Phelps & McNamara, P.C. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Hyman, Phelps & McNamara, P.C. has 4 FDA 510(k) cleared medical devices. Based in Woodland Hills, US.
Historical record: 4 cleared submissions from 1993 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Hyman, Phelps & McNamara, P.C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hyman, Phelps & McNamara, P.C.
4 devices