FDA 510(k) Applications Submitted by SCOTT E MOORE

FDA 510(k) Number Submission Date Device Name Applicant
K000189 01/21/2000 PQ1 ULTRADENT PRODUCTS, INC.
K992097 06/21/1999 ENDOREZ ULTRADENT PRODUCTS, INC.
K992380 07/16/1999 ENDO-EZE MOTOR AND HANDPIECE ULTRADENT PRODUCTS, INC.
K983668 10/19/1998 MODIFICATION OF PQ1 ULTRADENT PRODUCTS, INC.
K993846 11/12/1999 ULTRASEAL XT PLUS ULTRADENT PRODUCTS, INC.
K994261 12/17/1999 ULTRATEMP TEMPORARY POLYCARBOXYLATE CEMENT ULTRADENT PRODUCTS, INC.


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