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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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