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POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A)

Page Type
Cleared 510(K)
510(k) Number
K052161
510(k) Type
Special
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2005
Days to Decision
73 days
Submission Type
Summary

POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A)

Page Type
Cleared 510(K)
510(k) Number
K052161
510(k) Type
Special
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2005
Days to Decision
73 days
Submission Type
Summary