Optik

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933776OPTIK LAPAROSCOPEMarch 16, 1994
K926166COAST VIDEO ENDOSCOPIC IMAGING SYSTEMJune 1, 1993
K896404TITAMED ANTWERP SYSTEMApril 16, 1990
K896589MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERPDecember 27, 1989
K894557LIGHTSCOPE SETAugust 7, 1989
K894558MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SETAugust 7, 1989