Innotron of Oregon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innotron of Oregon, Inc. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Innotron of Oregon, Inc. has 28 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 28 cleared submissions from 1980 to 1990. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Innotron of Oregon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innotron of Oregon, Inc.
28 devices
Cleared
Aug 22, 1990
INNOFLUOR (TM) AMIKACIN CALIBRATOR SET
Toxicology
40d
Cleared
Aug 09, 1990
INNOFLUOR (TM) AMIKACIN REAGENT SET
Toxicology
27d
Cleared
Apr 20, 1990
MODIFIED ACCUFLUOR TOBRAMYCIN REAGENT & CALIBRATOR
Toxicology
67d
Cleared
Apr 19, 1990
MODIFIED ACCUFLUOR VANCOMYCIN REAGENT & CALIBRATOR
Toxicology
66d
Cleared
Apr 12, 1990
MODIFIED ACCUFLUOR CARBAMAZEPINE REAGENT & CALIBRA
Toxicology
59d
Cleared
Apr 12, 1990
MODIFIED ACCUFLUOR GENTAMICIN REAGENT & CALIBRATOR
Toxicology
59d
Cleared
Apr 12, 1990
MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA
Toxicology
59d
Cleared
Apr 12, 1990
MODIFIED ACCUFLUOR QUINIDINE REAGENT & CALIBRATOR
Toxicology
59d
Cleared
Apr 12, 1990
MODIFIED ACCUFLUOR THEOPHYLLINE REAGENT & CALIBRA
Toxicology
59d
Cleared
Oct 31, 1989
INNOFLUOR PHENYTOIN MANUAL FPIA REAGENT SET
Toxicology
29d
Cleared
Oct 30, 1989
INNOFLUOR DIGOXIN CALIBRATOR SET
Toxicology
28d
Cleared
Oct 30, 1989
INNOFLUOR DIGOXIN REAGENT SET
Toxicology
28d