Biocheck, Inc.
Biocheck, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2004, with 1 FDA device recall on record.
Top product codes for Biocheck, Inc.
FDA recalls by Biocheck, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Biocheck, Inc.
- K041619 — BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #801116
- K040030 — BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-804114
- K022660 — BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117
- K013062 — BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT
- K003851 — BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1119
- K002294 — BIOCHECK TESTOSTERONE EIA, MODEL BC-1115
- K001022 — BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061
- K992517 — BIOCHECK FERRITIN ELISA MODEL BC-1025
- K992528 — BIOCHECK IGE ELISA, MODEL BC-1035
- K991741 — BIOCHECK HCG ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1027
- K990993 — BIOCHECK SENSITIVE TSH (S-TSH) ENZYME IMMUNOASSAY TEST KIT; CATALOG NUMBER: BC-1003
- K991146 — TSH ENZYME IMMUNOASSAY TEST KIT, MODEL #BC-1001
- K991311 — TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005
- K991432 — BIOCHECK TOTAL T4 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1007
Data sourced from openFDA. This site is unofficial and independent of the FDA.