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HEARTSTREAM FR2 AED, MODEL M3860A,M3861A

Page Type
Cleared 510(K)
510(k) Number
K003565
510(k) Type
Special
Applicant
AGILENT TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2000
Days to Decision
30 days
Submission Type
Summary

HEARTSTREAM FR2 AED, MODEL M3860A,M3861A

Page Type
Cleared 510(K)
510(k) Number
K003565
510(k) Type
Special
Applicant
AGILENT TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2000
Days to Decision
30 days
Submission Type
Summary