FDA 510(k) Applications Submitted by MEDIGUIDE, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K091780 06/17/2009 GUIDED MEASUREMENT CATHETER (GMC) MEDIGUIDE, LTD.
K091781 06/17/2009 GUIDED MEDICAL POSITIONING SYSTEM (GMPS) MEDIGUIDE, LTD.
K102905 09/30/2010 GUIDED MEDICAL POSITIONING SYSTEM II (GMPS II) MEDIGUIDE, LTD.


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