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Cardio Medical Products

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1669-2013Class IICardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG ElectroApril 26, 2013

Recent 510(k) Clearances

K-NumberDeviceDate
K103651CARDIOMEDOctober 4, 2011
K103334CARDIO MEDJanuary 18, 2011
K103159CARDIO MED MODEL A102, H104, O101, P103, AND Z100January 11, 2011