Vistek Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vistek Corp. General & Plastic Surgery ✕
5 devices
Cleared
Dec 18, 1990
VLS 5300 300W XENON LIGHT SOURCE
General & Plastic Surgery
64d
Cleared
Dec 18, 1990
VISTEK ELECTRONIC CONTROLLER
General & Plastic Surgery
64d
Cleared
Apr 10, 1987
LCA 2000
General & Plastic Surgery
24d
Cleared
Feb 07, 1986
VIS-2000 VIDEO SYSTEM
General & Plastic Surgery
21d
Cleared
Dec 12, 1984
VIS-1000 VIDEO SYSTEM
General & Plastic Surgery
76d