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FDA 510(k) Applications Submitted by DANIEL CHER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091559
05/28/2009
MARKSMANN CATHETER
CHESTNUT MEDICAL TECHNOLOGIES, INC.
K093977
12/24/2009
ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX
CHESTNUT MEDICAL TECHNOLOGIES, INC.
K111490
05/31/2011
MARKSMAN CATHETER, *REFERS TO DIFFERENT CATHETER WORKING LENGHTS, DISTAL SINGLE COILED LENGTHS AND DISTAL SHAFT LENGTHS
EV3 INC
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