Ryder Intl. Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ryder Intl. Corp. Ophthalmic ✕
7 devices
Cleared
Sep 18, 1996
RYDER LACRIMAL INTUBATIONSET
Ophthalmic
106d
Cleared
Mar 04, 1992
OPTI-LENS CONTACT LENS CASE
Ophthalmic
57d
Cleared
Jan 13, 1992
OPTI-LENS(TM) CONTACT LENS CASE
Ophthalmic
62d
Cleared
Feb 20, 1987
CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695
Ophthalmic
24d
Cleared
Feb 07, 1986
KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)
Ophthalmic
154d
Cleared
Dec 13, 1985
KESTREL CONTACT LENS STORAGE CASE(NORYL)
Ophthalmic
98d
Cleared
Dec 13, 1985
KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)
Ophthalmic
98d