Medical Device Manufacturer · US , San Luis Obispo , CA

Phacor Inc., A Santen Company - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Phacor Inc., A Santen Company has 1 FDA 510(k) cleared medical devices. Based in San Luis Obispo, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Phacor Inc., A Santen Company Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Phacor Inc., A Santen Company

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