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SPIRIT 5000 CARDIAC COIL

Page Type
Cleared 510(K)
510(k) Number
K033490
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2004
Days to Decision
66 days
Submission Type
Summary

SPIRIT 5000 CARDIAC COIL

Page Type
Cleared 510(K)
510(k) Number
K033490
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2004
Days to Decision
66 days
Submission Type
Summary