FDA 510(k) Applications Submitted by REFERENCE DIAGNOSTICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030044 |
01/06/2003 |
EXTENDED RANGE HS CRP KIT, CAT NO:9200 |
REFERENCE DIAGNOSTICS, INC. |
| K990216 |
01/22/1999 |
MAGNETIC TIBC KIT |
REFERENCE DIAGNOSTICS, INC. |
| K000781 |
03/10/2000 |
DIRECT TIBC KIT |
REFERENCE DIAGNOSTICS, INC. |
| K000783 |
03/10/2000 |
DIRECT TIBC CALIBRATOR |
REFERENCE DIAGNOSTICS, INC. |
| K030772 |
03/11/2003 |
RDI EXTENDED RANGE CRP CALIBRATOR SET |
REFERENCE DIAGNOSTICS, INC. |
| K021607 |
05/16/2002 |
RDI HS CRP CALIBRATOR SET |
REFERENCE DIAGNOSTICS, INC. |
| K021609 |
05/16/2002 |
RDI HS CRP KIT |
REFERENCE DIAGNOSTICS, INC. |
| K052148 |
08/08/2005 |
TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET |
REFERENCE DIAGNOSTICS, INC. |
| K973988 |
10/21/1997 |
RDI HOMOGENEOUS HDL CHOLESTEROL TEST |
REFERENCE DIAGNOSTICS, INC. |
| K053211 |
11/16/2005 |
RDI HSFERRITIN KIT |
REFERENCE DIAGNOSTICS, INC. |
| K984107 |
11/17/1998 |
RDI DIRECT LDL CHOLESTEROL TEST |
REFERENCE DIAGNOSTICS, INC. |
| K053291 |
11/25/2005 |
FERRITIN CALIBRATOR SET, CATALOG NO. 8203 |
REFERENCE DIAGNOSTICS, INC. |
| K964063 |
10/10/1996 |
RDI LDL PRECIPITATION REAGENT |
REFERENCE DIAGNOSTICS, INC. |
| K964064 |
10/10/1996 |
RDI LIPIDIRECT MAGNETIC LDL REAGENT |
REFERENCE DIAGNOSTICS, INC. |
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