Visitec Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
49
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}October 12, 1995
K945114VISITEC SCLERAL PLUGFebruary 23, 1995
K945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEFebruary 14, 1995
K945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSJanuary 17, 1995
K942234VISITEC PRECISE-POINTJuly 12, 1994
K934269FIBEROPTIC ILLUMINATED INSTRUMENTSMay 17, 1994
K940210VISITEC EYE PADMarch 7, 1994
K933872VISI-SPEAR EYE SPONGEDecember 27, 1993
K923972OPHTHALMIC FLUID DISTRIBUTION SETSNovember 4, 1992
K922530VISITEC MICROSURGICAL SUTUREOctober 20, 1992
K923645VISITEC ASPIRATING SYRINGESeptember 30, 1992
K915808AQUEOUS PARACENTESIS PIPETMarch 19, 1992
K915809VISITEC CANALICULAR STENTFebruary 24, 1992
K910516DISPOSAL PAD FOR SHARPSApril 29, 1991
K904074VITREORETINAL INFUSION CANNULAFebruary 26, 1991
K902857VISI-DRAPE OPHTHALMIC DRAPESJuly 31, 1990
K902750VISI-SWAB OPHTALMIC SPONGEJuly 26, 1990
K902010VISI - STICK OPHTHALMIC SUTURE RETAINER TAPEJune 20, 1990
K900786VISI-SORB ABSORBANT STICKMay 18, 1990
K896622VISITEC VITRECTOMY UNITApril 4, 1990