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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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