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FDA 510(k) Applications Submitted by SIMBIONIX LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112387
08/18/2011
PROCEDURE REHEARSAL STUDIO(TM)
SIMBIONIX LTD.
K093269
10/19/2009
PROCEDURE REHEARSAL STUDIO
SIMBIONIX LTD.
K123269
10/19/2012
PROCEDURE REHEARSAL STUDIO
SIMBIONIX LTD.
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