Biocheck, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biocheck, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Biocheck, Inc. has 14 FDA 510(k) cleared chemistry devices. Based in Northridge, US.
Historical record: 14 cleared submissions from 1999 to 2004.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biocheck, Inc.
14 devices
Cleared
Dec 17, 2004
BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #801116
Chemistry
185d
Cleared
Jun 16, 2004
BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-804114
Immunology
161d
Cleared
Dec 19, 2002
BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117
Chemistry
132d
Cleared
Jan 08, 2002
BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT
Chemistry
118d
Cleared
Jul 20, 2001
BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT,...
Chemistry
220d
Cleared
Oct 02, 2000
BIOCHECK TESTOSTERONE EIA, MODEL BC-1115
Chemistry
67d
Cleared
Sep 26, 2000
BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061
Immunology
180d
Cleared
Sep 24, 1999
BIOCHECK FERRITIN ELISA MODEL BC-1025
Immunology
58d
Cleared
Sep 21, 1999
BIOCHECK IGE ELISA, MODEL BC-1035
Immunology
55d
Cleared
Jul 22, 1999
BIOCHECK HCG ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1027
Chemistry
62d
Cleared
Jun 22, 1999
BIOCHECK SENSITIVE TSH (S-TSH) ENZYME IMMUNOASSAY TEST KIT
Chemistry
90d
Cleared
Jun 22, 1999
TSH ENZYME IMMUNOASSAY TEST KIT, MODEL #BC-1001
Chemistry
78d