FDA 510(k) Applications Submitted by D T WOLF
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K982201 |
06/22/1998 |
ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE) |
FOREMOST DENTAL MFG., INC. |
K954867 |
10/24/1995 |
IONOSIT SEAL |
FOREMOST DENTAL MFG., INC. |
K970683 |
02/24/1997 |
ZENTIH FLOWABLE COMPOSITE (MULTIPLE) |
FOREMOST DENTAL MFG., INC. |
K970774 |
03/04/1997 |
TEMPOCEM NE (MULTIPLE) |
FOREMOST DENTAL MFG., INC. |
K970775 |
03/04/1997 |
TEMPO CEM (MULTIPLE) |
FOREMOST DENTAL MFG., INC. |
K990680 |
03/02/1999 |
DENTEC LD 15 DIODE LASER |
DENTEK LASERSYSTEMS PRODUKTIONS GES.M.B.H. |
K042687 |
09/29/2004 |
ENZYGNOST F+2 (MONOCLONAL) TEST KIT |
DADE BEHRING, INC. |
K020692 |
03/04/2002 |
EMIT 2000 VANCOMYCIN ASSAY |
DADE BEHRING, INC. |
K020845 |
03/15/2002 |
EMIT 2000 VANCOMYCIN CALIBRATORS |
DADE BEHRING, INC. |
K050665 |
03/15/2005 |
N ANTISERA TO HUMAN COMPLEMENT FACTORS (C3C, C4) |
DADE BEHRING, INC. |
K010871 |
03/23/2001 |
TGL FLEX REAGENT CARTRIDGE |
DADE BEHRING, INC. |
K001256 |
04/19/2000 |
CONTROL PLASMA N |
DADE BEHRING, INC. |
K021381 |
05/01/2002 |
MODIFICATION TO N/T RHEUMATOLOGY CONTROLS SL 1 & 2 |
DADE BEHRING, INC. |
K041870 |
07/09/2004 |
N APOLIPOPROTEIN STANDARD SERUM |
DADE BEHRING, INC. |
K022290 |
07/15/2002 |
PROTEIN S AC |
DADE BEHRING, INC. |
K042209 |
08/16/2004 |
CONTROL PLASMA N AND CONTROL PLASMA P |
DADE BEHRING, INC. |
K023141 |
09/20/2002 |
MODIFICATION TO STANDARD HUMAN PLASMA |
DADE BEHRING, INC. |
K023309 |
10/03/2002 |
CONTROL PLASMA N |
DADE BEHRING, INC. |
K023312 |
10/03/2002 |
CONTROL PLASMA P |
DADE BEHRING, INC. |
K993310 |
10/04/1999 |
APOLIPOPROTEIN CONTROL SERUM CHD, MODEL OUPH |
DADE BEHRING, INC. |
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