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VISION 9000 PHASED ARRAY TORSO COIL

Page Type
Cleared 510(K)
510(k) Number
K002482
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2000
Days to Decision
64 days
Submission Type
Summary

VISION 9000 PHASED ARRAY TORSO COIL

Page Type
Cleared 510(K)
510(k) Number
K002482
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2000
Days to Decision
64 days
Submission Type
Summary