FDA 510(k) Applications Submitted by DANIEL R SCHECHTER, ESQ

FDA 510(k) Number Submission Date Device Name Applicant
K101044 04/14/2010 RETRIEVE IMPLANT CEMENT PARKELL, INC.
K022097 06/27/2002 THERMIQUE PARKELL, INC.
K002195 07/20/2000 FORAMATRON V, MODEL D680 PARKELL, INC.
K063003 10/02/2006 AURORA PARKELL, INC.
K113839 12/28/2011 RETRACT GINGIVAL RETRACTION/HEMOSTATIC PASTE PARKELL, INC.
K073698 12/31/2007 SECURE PARKELL, INC.
K080549 02/27/2008 DURAFINISH ALL-CURE, MODEL S296 PARKELL, INC.


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