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Cortek Endoscopy, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K000199CORTEK MINI LAPAROSCOPEApril 13, 2000
K000198CORTEK ARTHROSCOPEApril 11, 2000
K000202CORTEK LAPAROSCOPESMarch 31, 2000
K000197CORTEK CYSTOSCOPEMarch 3, 2000
K000200CORTEK URETHEROSCOPEMarch 3, 2000