FDA 510(k) Applications Submitted by JOHN DISCKO

FDA 510(k) Number Submission Date Device Name Applicant
K010133 01/17/2001 VERSALUX CENTRIX, INC.
K980568 02/09/1998 JUMBO GLASS IONOMER CEMENT CENTRIX, INC.
K961190 03/26/1996 GLY-ETCH CENTRIX, INC.
K971121 03/27/1997 ENCORE BOND CENTRIX, INC.
K021131 04/08/2002 CHLORAPREP CENTRIX, INC.
K021146 04/09/2002 D/SENSE 1-STEP CENTRIX, INC.
K091380 05/11/2009 CORDCAP CENTRIX, INC.
K111348 05/13/2011 RE / STASIS (TM) GINGIVAL RETRACTION PASTE CENTRIX, INC.
K981972 06/04/1998 GREEN-OR DENTIN DESENSITIZER CENTRIX, INC.
K982665 07/24/1998 JUMBO SILVER-REINFORCED GLASS IONOMER CENTRIX, INC.
K992629 07/28/1999 D/SENSE II (GREEN-OR) DENTIN DESENSITIZER CENTRIX, INC.
K963311 08/22/1996 TEAM ETCH CENTRIX, INC.
K973257 08/29/1997 VERSAETCH CENTRIX, INC.
K973285 09/02/1997 D/SENSE-T CENTRIX, INC.
K963927 09/10/1996 TEAM CARIES INDICATOR CENTRIX, INC.
K964735 11/25/1996 DENTINSENSE CENTRIX, INC.
K965138 12/23/1996 DENTINSENSE B/C CENTRIX, INC.


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