FDA 510(k) Applications Submitted by ANDERJEET S 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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