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POWERHEART AED G3A

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040438
510(k) Type
Traditional
Applicant
Cardiac Science, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2004
Days to Decision
133 days
Submission Type
Summary

POWERHEART AED G3A

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040438
510(k) Type
Traditional
Applicant
Cardiac Science, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2004
Days to Decision
133 days
Submission Type
Summary