Medical Device Manufacturer · US , San Francisco , CA

Altex Vision - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Altex Vision has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Altex Vision Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Altex Vision

2 devices
1-2 of 2
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All2 Ophthalmic 2