Last synced on 14 November 2025 at 11:06 pm

POWERHEART CARDIAC RHYTHM MODULE

Page Type
Cleared 510(K)
510(k) Number
K012197
510(k) Type
Traditional
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
126 days
Submission Type
Summary

POWERHEART CARDIAC RHYTHM MODULE

Page Type
Cleared 510(K)
510(k) Number
K012197
510(k) Type
Traditional
Applicant
CARDIAC SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
126 days
Submission Type
Summary