Medical Device Manufacturer · US , Milford , CT

Micro Specialties, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1998

Recent clearances: M2 COMPATIBLE MICROKERATOME BLADE, KERATOME BLADE 200200 & 600600, KERATOME BLADE, CHIROM MODEL ALK 500500

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Micro Specialties, Inc. Ophthalmic ✕

4 devices

1-4 of 4

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