FDA 510(k) Applications Submitted by LINDA STUNDTNER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020596 |
02/22/2002 |
CALIBRATING MATERIAL,CAL-PAK, CAL & SLOPE STANDARDS |
DIAMOND DIAGNOSTICS, INC. |
| K020894 |
03/19/2002 |
CALIBRATING MATERIAL, CAL-PAK, BUFFERS |
MISSION DIAGNOSTICS |
| K022027 |
06/21/2002 |
CALIBRATING MATERIAL, BUFFERS, STANDARD |
MISSION DIAGNOSTICS |
| K033055 |
09/29/2003 |
GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS |
DIAMOND DIAGNOSTICS, INC. |
| K031159 |
04/14/2003 |
CALIBRATING MATERIAL, CALIBRATING STANDARDS |
DIAMOND DIAGNOSTICS, INC. |
| K033056 |
09/29/2003 |
BUN REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA REAGENT |
DIAMOND DIAGNOSTICS, INC. |
| K033058 |
09/29/2003 |
CREATININE REAGENT KIT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS |
DIAMOND DIAGNOSTICS, INC. |
| K033060 |
09/29/2003 |
CALIBRATING MATERIAL, CALIBRATING STANDARDS |
DIAMOND DIAGNOSTICS, INC. |
| K033061 |
09/29/2003 |
CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE |
DIAMOND DIAGNOSTICS, INC. |
| K033063 |
09/29/2003 |
MISSION CONTROLS |
DIAMOND DIAGNOSTICS, INC. |
| K013850 |
11/20/2001 |
STANDARD A, STANDARD B, STANDARD C, CAL, SLOPE |
DIAMOND DIAGNOSTICS, INC. |
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