FDA 510(k) Applications Submitted by TOKUYAMA AMERICA, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K980051 |
01/06/1998 |
PALFIQUE ESTELITE PASTE |
TOKUYAMA AMERICA, INC. |
K980054 |
01/06/1998 |
PALFIQUE ESTELITE |
TOKUYAMA AMERICA, INC. |
K980058 |
01/06/1998 |
TOKUSO MAC BOND II |
TOKUYAMA AMERICA, INC. |
K010267 |
01/29/2001 |
PALFIQUE ESTELITE LV CLEAR |
TOKUYAMA AMERICA, INC. |
K991711 |
05/19/1999 |
BISTITE II SC |
TOKUYAMA AMERICA, INC. |
K011685 |
05/31/2001 |
BISTITE II DC |
TOKUYAMA AMERICA, INC. |
K011854 |
06/13/2001 |
TOKUYAMA M-BOND |
TOKUYAMA AMERICA, INC. |
K982537 |
07/21/1998 |
TOKUYAMA SOFRELINER |
TOKUYAMA AMERICA, INC. |
K953589 |
08/01/1995 |
TOKUYAMA SOFT RELINING |
TOKUYAMA AMERICA, INC. |
K022641 |
08/08/2002 |
TOKUYAMA REBASE II |
TOKUYAMA AMERICA, INC. |
K973245 |
08/29/1997 |
TOKUSO REBASE MR. BOND |
TOKUYAMA AMERICA, INC. |
K002863 |
09/13/2000 |
PALFIQUE ESTELITE LV |
TOKUYAMA AMERICA, INC. |
K993917 |
11/17/1999 |
TOKUYAMA ONE-UP-BOND F |
TOKUYAMA AMERICA, INC. |
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