FDA 510(k) Applications Submitted by LORI ROBINSON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K981012 |
03/18/1998 |
AIA-PACK MYOGLOBIN ASSAY |
TOSOH MEDICS, INC. |
| K971103 |
03/26/1997 |
AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEM |
TOSOH MEDICS, INC. |
| K951848 |
04/21/1995 |
AIA-PACK CPR ASSAY |
TOSOH MEDICS, INC. |
| K981522 |
04/28/1998 |
AIA-PACK TGAB ASSAY |
TOSOH MEDICS, INC. |
| K972265 |
06/17/1997 |
A1C 2.2 PLUS - AUTOMATED GLYCOHEMOGLOBIN ANALYZER |
TOSOH MEDICS, INC. |
| K972586 |
07/11/1997 |
AIA-PACK TSH 3RD-GEN ASSAY |
TOSOH MEDICS, INC. |
| K972697 |
07/18/1997 |
AIA-PACK IGE II ASSAY |
TOSOH MEDICS, INC. |
| K963687 |
09/16/1996 |
AIA-PACK FT3 ASSAY |
TOSOH MEDICS, INC. |
| K964348 |
10/31/1996 |
AIA-PACK B12 ASSAY |
TOSOH MEDICS, INC. |
| K964349 |
10/31/1996 |
AIA-PACK FOLATE ASSAY |
TOSOH MEDICS, INC. |
| K984359 |
12/07/1998 |
AIA-PACK TROPONIN I ASSAY |
TOSOH MEDICS, INC. |
|
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