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FIDELITY 200 CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K071228
510(k) Type
Abbreviated
Applicant
SIGNALIFE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
202 days
Submission Type
Summary

FIDELITY 200 CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K071228
510(k) Type
Abbreviated
Applicant
SIGNALIFE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
202 days
Submission Type
Summary