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LIBERTY 9000 BREAST COIL

Page Type
Cleared 510(K)
510(k) Number
K000993
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2000
Days to Decision
59 days
Submission Type
Summary

LIBERTY 9000 BREAST COIL

Page Type
Cleared 510(K)
510(k) Number
K000993
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2000
Days to Decision
59 days
Submission Type
Summary