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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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