FDA 510(k) Applications Submitted by PHOENIX DIAGNOSTICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020129 |
01/14/2002 |
PHOENIX ELETROLYTE CALIBRATION SET FOR THE ROCHE COBAS ISE MODULE |
PHOENIX DIAGNOSTICS, INC. |
| K020148 |
01/16/2002 |
pHoenix ISE Reagents FOR Olympus AU Chemistry Systems |
PHOENIX DIAGNOSTICS, INC. |
| K960592 |
02/12/1996 |
ELECTROLYTE STANDARDS |
PHOENIX DIAGNOSTICS, INC. |
| K012509 |
08/06/2001 |
PHOENIX ELECTROLYTE CALIBRATION SET FOR THE DADE/BEHRING/BEHRING DIMENSION CHEMISTRY SYSTEM |
PHOENIX DIAGNOSTICS, INC. |
| K012987 |
09/06/2001 |
PHOENIX ELECTROLYTE CALIBRATION SET FOR THE MEDICAL EASYLYTE CALCIUM ANALYZER |
PHOENIX DIAGNOSTICS, INC. |
| K023268 |
09/30/2002 |
PHOENIX ISE STANDARD A,B AND C FOR ROCHE/AVL SYSTEMS |
PHOENIX DIAGNOSTICS, INC. |
| K013451 |
10/18/2001 |
PHOENOIX ISE REAGENTS FOR ROCHE HITACHI, MODELS 700/900 SERIES |
PHOENIX DIAGNOSTICS, INC. |
| K020364 |
02/04/2002 |
PHOENIX ISE REAGENTS FOR BECKMAN CX SYSTEMS |
PHOENIX DIAGNOSTICS, INC. |
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