Biohytech International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biohytech International, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Biohytech International, Inc. has 7 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 7 cleared submissions from 1986 to 1987. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Biohytech International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biohytech International, Inc.
7 devices
Cleared
Mar 24, 1987
DS-DNA EIA DIAGNOSTIC KIT
Immunology
62d
Cleared
Mar 17, 1987
SS-DNA EIA DIAGNOSTIC KIT
Immunology
55d
Cleared
Mar 17, 1987
SM EIA DIAGNOSTIC KIT
Immunology
55d
Cleared
Mar 17, 1987
DNP EIA DIAGNOSTIC KIT
Immunology
55d
Cleared
Mar 17, 1987
RNP EIA DIAGNOSTIC KIT
Immunology
55d
Cleared
Mar 17, 1987
HISTONES EIA DIAGNOSTIC KIT
Immunology
55d
Cleared
Oct 24, 1986
ANA-ENZYME IMMUNOASSAY (ANA-EIA) DIAGNOSTIC KIT
Immunology
79d