Medical Device Manufacturer · US , Milford , CT

Insight Technologies Instruments, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Recent clearances: KERATOME SYSTEM, MODEL K3000, KERATOME SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Insight Technologies Instruments, LLC Ophthalmic ✕

2 devices

1-2 of 2

Cleared May 14, 1999

KERATOME SYSTEM, MODEL K3000

Ophthalmic · 144d

Cleared Jan 20, 1998

KERATOME SYSTEM

Ophthalmic · 69d