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POWERHEART AED G3, MODEL 9300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031987
510(k) Type
Special
Applicant
CARDIAC SCIENCE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
33 days
Submission Type
Summary

POWERHEART AED G3, MODEL 9300

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031987
510(k) Type
Special
Applicant
CARDIAC SCIENCE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
33 days
Submission Type
Summary