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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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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