FDA 510(k) Applications Submitted by STEVE RUDOLPH

FDA 510(k) Number Submission Date Device Name Applicant
K040343 02/12/2004 TEMP F NOVOCOL, INC.
K120619 02/29/2012 ORTHODONTIC FLOWABLE BRACKET ADHESIVE NOVOCOL, INC.
K101540 06/03/2010 GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE NOVOCOL INC. DBA SEPTODONT AND CONFI-DENTAL PRODUC
K072150 08/03/2007 DIMER ACID DERIVED NANO-HYBRID COMPOSITE RESTORATIVE MATERIAL NOVOCOL, INC.
K092501 08/14/2009 LIGHT-ACTIVATED LOW-STRESS THIOL-ENE COMPOSITE RESTORATIVE MATERIAL NOVOCOL, INC.


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