Siegel,Mandell & Davidson,P.C. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siegel,Mandell & Davidson,P.C. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Siegel,Mandell & Davidson,P.C. has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 4 cleared submissions from 1994 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Siegel,Mandell & Davidson,P.C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Siegel,Mandell & Davidson,P.C.
5 devices
Cleared
May 02, 1995
POWER RANGERS SUNGLASSES
Ophthalmic
57d
Cleared
Apr 05, 1995
AVON MASSAGING HAIRBRUSH
Physical Medicine
35d
Cleared
Jan 31, 1995
AVON SUNNY DAYS SUNGLASSES
Ophthalmic
48d
Cleared
Jan 31, 1995
AVON SUNNY DAYS SUNGLASSES
Ophthalmic
48d
Cleared
May 17, 1994
AVON CAT SUNGLASSES
Ophthalmic
57d