Medical Device Manufacturer · US , Greenwood Village , CO

Sie Ag,Surgical Instument Engineering - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Recent clearances: FEMTO LDV

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sie Ag,Surgical Instument Engineering Ophthalmic ✕

1 devices

1-1 of 1

Cleared Mar 16, 2012

Ophthalmic · 233d