Medical Device Manufacturer · US , Tustin , CA

Surgin, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Recent clearances: PRIZM KERATOME BLADE (NIDEK MODEL), MODEL MK8514NI

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Dec 13, 2001

PRIZM KERATOME BLADE (NIDEK MODEL), MODEL MK8514NI

Ophthalmic · 65d