FDA 510(k) Applications Submitted by LYNDA M TAYLOR
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K970509 |
02/11/1997 |
INNOFLOUR CALIBRATOR REAGENT SET |
OXIS INTL., INC. |
K970510 |
02/11/1997 |
INNOFLOUR TOPIRAMATE REAGENT SET |
OXIS INTL., INC. |
K970517 |
02/11/1997 |
INNOFLUOR TOPIRAMATE CONTROL SET |
OXIS INTL., INC. |
K972330 |
06/23/1997 |
INNOFLUOR PHENOBARBITAL ASSAY SYSTEM |
OXIS INTL., INC. |
K972331 |
06/23/1997 |
INNOFLUOR GENTAMICIN ASSAY SYSTEM |
OXIS INTL., INC. |
K955562 |
12/06/1995 |
INNOFLUOR PHENYTOIN ASSAY SYSTEM |
OXIS INTL., INC. |
K955567 |
12/06/1995 |
INNOFLUOR THEOPHYLLINE ASSAY SYSTEM |
OXIS INTL., INC. |
K955568 |
12/06/1995 |
INNOFLUOR QUINIDINE ASSAY SYSTEM |
OXIS INTL., INC. |
K955569 |
12/06/1995 |
INNOFLUOR GENTAMICIN ASSAY SYSTEM |
OXIS INTL., INC. |
K955570 |
12/06/1995 |
INNOFLUOR AMIKACIN ASSAY SYSTEM |
OXIS INTL., INC. |
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