FDA 510(k) Applications Submitted by RAYMOND J KELLY IV

FDA 510(k) Number Submission Date Device Name Applicant
K130424 02/20/2013 STIMEL-03 STIMEL LTD
K100595 03/02/2010 ECLERIS MICROSTAR COLPOSCOPE Ecleris USA
K131045 04/15/2013 ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE CARDIAC DESIGNS, LLC
K131323 05/08/2013 ECLERIS SINUSCOPE Ecleris USA
K132899 09/16/2013 EQUASHIELD CLOSED SYSTEM DRUG TRANSFER DEVICE (CSTD) EQUASHIELD MEDICAL LTD


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