Sangui Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sangui Biotech, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sangui Biotech, Inc. has 5 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Historical record: 5 cleared submissions from 1997 to 2000. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Sangui Biotech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sangui Biotech, Inc.
5 devices
Cleared
Aug 23, 2000
CHRONALCO I.D.CDT (CARBOHYDRATE DEFICIENT TRANSFERRIN) ASSAY
Chemistry
58d
Cleared
Jun 07, 2000
SANGUI BIOTECH, INC. EPO (ERYTHROPOIETIN) ELISA KIT
Hematology
293d
Cleared
Sep 03, 1998
SANGUI BIOTECH, INC. CALCITONIN ELISA KIT
Chemistry
48d
Cleared
Aug 19, 1998
SANGUI BIOTECH, INC. ACTH (ADRENOCORTICOTROPIC HORMONE) ELISA KIT
Chemistry
23d
Cleared
Dec 23, 1997
SANGUI BIOTECH, INC. INTACT-PTH (PARATHYROID HORMONE) ELISA
Chemistry
36d