FDA 510(k) Applications Submitted by ROBIN C HART
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K972386 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA O GROUP B |
LEE LABORATORIES, INC. |
| K972387 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA O GROUP A |
LEE LABORATORIES, INC. |
| K972388 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA O GROUP C |
LEE LABORATORIES, INC. |
| K972389 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA H D |
LEE LABORATORIES, INC. |
| K972390 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA H C |
LEE LABORATORIES, INC. |
| K972391 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA H B |
LEE LABORATORIES, INC. |
| K972392 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA H A |
LEE LABORATORIES, INC. |
| K972394 |
06/26/1997 |
VISTA ANTIGEN BRUCELLA ABORTUS |
LEE LABORATORIES, INC. |
| K972395 |
06/26/1997 |
VISTA ANTIGEN SALMONELLA O GROUP D |
LEE LABORATORIES, INC. |
| K972396 |
06/26/1997 |
VISTA ANTIGEN BRUCELLA MELITENSIS |
LEE LABORATORIES, INC. |
| K071799 |
07/02/2007 |
MODIFICATION TO BIOSTAR OIA SHIGATOX |
IVERNESS MEDICAL PROFESSIONAL DIAGNOSTICS |
| K061889 |
07/03/2006 |
BIOSTAR OIA SHIGATOX |
INVERNESS MEDICAL-BIOSTAR INC. |
|
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