FDA 510(k) Applications Submitted by JONATHAN WARD

FDA 510(k) Number Submission Date Device Name Applicant
K121009 04/03/2012 HEARTCHECK ECG PEN WITH GEMS HOME CARDIO COMM SOLUTIONS, INC.
K111159 04/25/2011 HEARTCHECK PEN HANDHELD ECG WITH GEMS HOME CARDIO COMM SOLUTIONS, INC.
K131384 05/14/2013 KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE KERICURE INC.
K092033 07/06/2009 VIBROLITH AND VIBROLITH PLUS INTRACORPOREAL LITHOTRIPTOR ELMED USA
K122632 08/29/2012 GUAVA II CARDIOCOMM SOLUTIONS, INC.
K082910 09/30/2008 CVS SILVER BANDAGES, WALGREENS SILVER BANDAGES, XYZ SILVER BANDAGES ASO LLC
K030891 03/21/2003 SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK SURGISTAR, INC.
K961524 04/22/1996 STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS STERILAB, INC.
K992978 09/03/1999 RICROKERATOME BLADE SURGISTAR, INC.


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