FDA 510(k) Applications Submitted by ANDY GULATI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K010250 |
01/26/2001 |
TETRIC CERAM HB |
IVOCLAR NORTH AMERICA, INC. |
| K010381 |
02/08/2001 |
D.SIGN 30 |
IVOCLAR NORTH AMERICA, INC. |
| K011022 |
04/04/2001 |
BIOUNIVERSAL PDF |
IVOCLAR NORTH AMERICA, INC. |
| K011023 |
04/04/2001 |
D.SIGN 96 |
IVOCLAR NORTH AMERICA, INC. |
| K002872 |
09/14/2000 |
R&D PROJECT DW271#11A |
IVOCLAR NORTH AMERICA, INC. |
| K003293 |
10/20/2000 |
EXCITE DSC |
IVOCLAR NORTH AMERICA, INC. |
| K003373 |
10/30/2000 |
PROCAD ADD-ON |
IVOCLAR NORTH AMERICA, INC. |
| K003374 |
10/30/2000 |
FERMIT PLUS |
IVOCLAR NORTH AMERICA, INC. |
| K003377 |
10/30/2000 |
FERMIT N PLUS |
IVOCLAR NORTH AMERICA, INC. |
| K003407 |
11/01/2000 |
SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER) |
IVOCLAR NORTH AMERICA, INC. |
| K003632 |
11/24/2000 |
DW 273 #1 |
IVOCLAR NORTH AMERICA, INC. |
| K003633 |
11/24/2000 |
DW 277 #4 |
IVOCLAR NORTH AMERICA, INC. |
| K003634 |
11/24/2000 |
DW 272 #1 |
IVOCLAR NORTH AMERICA, INC. |
| K003635 |
11/24/2000 |
DW 276 #3 |
IVOCLAR NORTH AMERICA, INC. |
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