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INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PELVIS COIL

Page Type
Cleared 510(K)
510(k) Number
K001209
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2000
Days to Decision
48 days
Submission Type
Summary

INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PELVIS COIL

Page Type
Cleared 510(K)
510(k) Number
K001209
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2000
Days to Decision
48 days
Submission Type
Summary