Oxis Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oxis Intl., Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Oxis Intl., Inc. has 11 FDA 510(k) cleared toxicology devices. Based in Portland, US.
Historical record: 11 cleared submissions from 1995 to 1997.
Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oxis Intl., Inc.
11 devices
Cleared
Aug 01, 1997
INNOFLUOR GENTAMICIN ASSAY SYSTEM
Toxicology
39d
Cleared
Jul 14, 1997
INNOFLUOR PHENOBARBITAL ASSAY SYSTEM
Toxicology
21d
Cleared
May 12, 1997
INNOFLOUR CALIBRATOR REAGENT SET
Toxicology
90d
Cleared
May 12, 1997
INNOFLOUR TOPIRAMATE REAGENT SET
Toxicology
90d
Cleared
May 12, 1997
INNOFLUOR TOPIRAMATE CONTROL SET
Toxicology
90d
Cleared
Apr 04, 1996
INNOFLUOR QUINIDINE ASSAY SYSTEM
Toxicology
120d
Cleared
Feb 09, 1996
INNOFLUOR GENTAMICIN ASSAY SYSTEM
Toxicology
65d
Cleared
Feb 09, 1996
INNOFLUOR AMIKACIN ASSAY SYSTEM
Toxicology
65d
Cleared
Jan 24, 1996
INNOFLUOR PHENYTOIN ASSAY SYSTEM
Toxicology
49d
Cleared
Jan 24, 1996
INNOFLUOR THEOPHYLLINE ASSAY SYSTEM
Toxicology
49d
Cleared
May 05, 1995
B-L RED(TM) DISCS
Microbiology
98d