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POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

Page Type
Cleared 510(K)
510(k) Number
K102496
510(k) Type
Special
Applicant
CARDIAC SCIENCE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2011
Days to Decision
282 days
Submission Type
Summary

POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

Page Type
Cleared 510(K)
510(k) Number
K102496
510(k) Type
Special
Applicant
CARDIAC SCIENCE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2011
Days to Decision
282 days
Submission Type
Summary