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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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