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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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