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FDA 510(k) Applications Submitted by CROSPON, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110529
02/24/2011
ENDOFLIP GASTRIC TUBE
CROSPON, LTD.
K110531
02/24/2011
ENDOFLIP ECD
CROSPON, LTD.
K130906
04/01/2013
ENDOFLIP CATHETER
CROSPON, LTD.
K120997
04/02/2012
BAROSTAT SOFTWARE OPTION
CROSPON, LTD.
K142000
07/23/2014
ESOFLIP ES
CROSPON, LTD.
K132337
07/26/2013
ESOFLIP BALLOON DILATION CATHETER
CROSPON, LTD.
K102214
08/06/2010
ENDO FLIP
CROSPON, LTD.
K092850
09/16/2009
ENDOFLIP
CROSPON, LTD.
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