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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact