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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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