Medical Device Manufacturer · JP , Komaki

Santec Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Recent clearances: ARGOS, ARGOS

2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Santec Corporation Ophthalmic ✕

2 devices
1-2 of 2
Cleared May 16, 2019
ARGOS
K191051 · MXK
Ophthalmic · 27d
Cleared Oct 02, 2015
ARGOS
K150754 · MXK
Ophthalmic · 193d
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