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PHASED ARRAY KNEE AND FOOT COIL

Page Type
Cleared 510(K)
510(k) Number
K994040
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
50 days
Submission Type
Summary

PHASED ARRAY KNEE AND FOOT COIL

Page Type
Cleared 510(K)
510(k) Number
K994040
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
50 days
Submission Type
Summary