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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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