Medical Device Manufacturer · US , San Clemente , CA

Glaukos - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Recent clearances: iPrime Viscodelivery System

View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Glaukos Ophthalmic ✕

1 devices
1-1 of 1
Cleared Jan 06, 2022
iPrime Viscodelivery System
K212797 · MRH
Ophthalmic · 126d
Filters
Filter by Specialty
All1 Ophthalmic 1