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SPIRIT III TOTALSENSE CARDIAC COIL

Page Type
Cleared 510(K)
510(k) Number
K024187
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2003
Days to Decision
47 days
Submission Type
Summary

SPIRIT III TOTALSENSE CARDIAC COIL

Page Type
Cleared 510(K)
510(k) Number
K024187
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2003
Days to Decision
47 days
Submission Type
Summary