Intl. Bioclinical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Bioclinical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Intl. Bioclinical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 6 cleared submissions from 1986 to 1991. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Intl. Bioclinical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Bioclinical, Inc.
6 devices
Cleared
Sep 23, 1991
INNOFLUOR(TM) DIGITOXIN REAGENT SET
Toxicology
67d
Cleared
Aug 30, 1991
INNOFLUOR(TM) DIGITOXIN CALIBRATOR SET
Toxicology
43d
Cleared
Jul 05, 1991
INNOFLUOR(TM) VALPROIC ACID REAGENT SET
Toxicology
80d
Cleared
May 23, 1991
INNOFLUOR VALPROIC ACID CALIBRATOR SET
Chemistry
50d
Cleared
Dec 15, 1988
ABC FP ANALYZER
Chemistry
119d
Cleared
Nov 24, 1986
PROGESTERONE SYSTEM BY EIA
Chemistry
32d