Visx, Incorporated is one of 23683 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visx, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: VISX CUSTOMVUE SLIT ILLUMINATOR WITH DESKTOP CHARGER, MODEL CV SI-1, WAVESCAN WAVEFRONT SYSTEM MODEL HS 1
2
Total
1
Cleared
0
Denied
Visx, Incorporated has 1 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 1 cleared submissions from 2000 to 2005. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Visx, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Visx, Incorporated
2 devices