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LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041695
510(k) Type
Special
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2004
Days to Decision
31 days
Submission Type
Summary