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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