FDA 510(k) Applications Submitted by APEX MEDICAL TECHNOLOGIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K112165 07/28/2011 RHEA CUP APEX MEDICAL TECHNOLOGIES, INC.
K954791 10/18/1995 SEMINAL FLUID COLLECTION KIT II APEX MEDICAL TECHNOLOGIES, INC.
K060933 04/05/2006 SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM APEX MEDICAL TECHNOLOGIES, INC.


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