Visioncare Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROCARE PLUS VITRECTOMY SYSTEM, BAYERS BIMANUAL I/A HANDPIECES
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Visioncare Devices, Inc. Ophthalmic ✕
5 devices
Cleared
May 30, 2012
PROCARE PLUS VITRECTOMY SYSTEM
Ophthalmic
132d
Cleared
Apr 17, 2003
VELOCITY ADVANTAGE
Ophthalmic
142d
Cleared
Jun 09, 1997
BAYERS BIMANUAL I/A HANDPIECES
Ophthalmic
77d
Cleared
Jun 06, 1994
VIT CUTTER MODEL 94
Ophthalmic
108d
Cleared
Jan 28, 1991
I/A VITROPHAGE MODEL YPR 2001
Ophthalmic
89d