FDA 510(k) Applications Submitted by DOLLY MISTRY

FDA 510(k) Number Submission Date Device Name Applicant
K130725 03/18/2013 MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR. COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
K091449 05/18/2009 DATASCOPE'S 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MODELS 0684,00-0498-01, 02 DATASCOPE CORP., CARDIAC ASSIST DIVISION
K132567 08/15/2013 ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER SINGLE LUMEN, ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER DUAL LUMEN COVIDIEN


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