Oxis Intl., Inc.
Oxis Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1997.
Top product codes for Oxis Intl., Inc.
Recent clearances by Oxis Intl., Inc.
- K972331 — INNOFLUOR GENTAMICIN ASSAY SYSTEM
- K972330 — INNOFLUOR PHENOBARBITAL ASSAY SYSTEM
- K970509 — INNOFLOUR CALIBRATOR REAGENT SET
- K970510 — INNOFLOUR TOPIRAMATE REAGENT SET
- K970517 — INNOFLUOR TOPIRAMATE CONTROL SET
- K955568 — INNOFLUOR QUINIDINE ASSAY SYSTEM
- K955569 — INNOFLUOR GENTAMICIN ASSAY SYSTEM
- K955570 — INNOFLUOR AMIKACIN ASSAY SYSTEM
- K955562 — INNOFLUOR PHENYTOIN ASSAY SYSTEM
- K955567 — INNOFLUOR THEOPHYLLINE ASSAY SYSTEM
- K950346 — B-L RED(TM) DISCS
Data sourced from openFDA. This site is unofficial and independent of the FDA.