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POWERHEART AED G3 PRO

Page Type
Cleared 510(K)
510(k) Number
K040637
510(k) Type
Traditional
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2004
Days to Decision
149 days
Submission Type
Summary

POWERHEART AED G3 PRO

Page Type
Cleared 510(K)
510(k) Number
K040637
510(k) Type
Traditional
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2004
Days to Decision
149 days
Submission Type
Summary