Last synced on 14 November 2025 at 11:06 pm

POWERHEART AED G3, MODEL 9300

Page Type
Cleared 510(K)
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)
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