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Cardio-Optics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K062340CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEMNovember 30, 2006
K050808CORONARY SINUS ACCESS KIT, MODEL KCS8F-01July 28, 2005