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PRIMA III TOTALSENSE TORSO COIL

Page Type
Cleared 510(K)
510(k) Number
K030371
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2003
Days to Decision
90 days
Submission Type
Summary

PRIMA III TOTALSENSE TORSO COIL

Page Type
Cleared 510(K)
510(k) Number
K030371
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2003
Days to Decision
90 days
Submission Type
Summary