Micro Specialties, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Micro Specialties, Inc. Ophthalmic ✕
4 devices
Cleared
May 25, 2004
M2 COMPATIBLE MICROKERATOME BLADE
Ophthalmic
208d
Cleared
Dec 16, 2002
KERATOME BLADE 200200 & 600600
Ophthalmic
306d
Cleared
May 01, 1998
KERATOME BLADE, CHIROM MODEL ALK 500500
Ophthalmic
80d
Cleared
May 01, 1998
KERATOME BLADE (135 MICRON, MODEL 300135), (160 MICRON, MODEL 300160), (200...
Ophthalmic
80d