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BODY ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K013594
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2002
Days to Decision
84 days
Submission Type
Summary

BODY ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K013594
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2002
Days to Decision
84 days
Submission Type
Summary