FDA 510(k) Applications Submitted by ANDERJEET GULATI

FDA 510(k) Number Submission Date Device Name Applicant
K020183 01/18/2002 PISCES PLUS (DW286 C) IVOCLAR VIVADENT, INC.
K020253 01/24/2002 4 ALL (DW286A) IVOCLAR VIVADENT, INC.
K020898 01/24/2002 D.SIGN 15 (DW286 B) IVOCLAR VIVADENT, INC.
K030435 02/10/2003 BIOUNIVERSAL PKF IVOCLAR VIVADENT, INC.
K030436 02/10/2003 BIO UNIVERSAL IVOCLAR VIVADENT, INC.
K011491 05/15/2001 HELIOSEAL CLEAR CHROMA IVOCLAR NORTH AMERICA, INC.
K011492 05/15/2001 IN TEN-S IVOCLAR NORTH AMERICA, INC.
K041433 05/28/2004 BRIGHT GOLD XH IVOCLAR VIVADENT, INC.
K021892 06/07/2002 BRIGHT GOLD IVOCLAR VIVADENT, INC.
K022811 08/23/2002 W-5 IVOCLAR VIVADENT, INC.
K012877 08/27/2001 HIGH GOLD PALLADIUM FREE CERAMIC SOLDER IVOCLAR USA, INC.
K032715 09/02/2003 DW 296 #15 SOLDER IVOCLAR VIVADENT, INC.
K022969 09/06/2002 UNIVERSAL CERAMIC SOLDER IVOCLAR VIVADENT, INC.
K013809 11/15/2001 D.SIGN 59 IVOCLAR VIVADENT, INC.
K032493 08/12/2003 ALEXANDER IVOCLAR VIVADENT, INC.
K062713 09/11/2006 ADHESIVE DC ACTIVATOR IVOCLAR VIVADENT, INC.
K014042 12/07/2001 D.SIGN 84 IVOCLAR VIVADENT, INC.


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