FDA 510(k) Applications Submitted by CIBERNET SYSTEMS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K050951 04/15/2005 MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370 CIBERNET SYSTEMS CORP.


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