Breit Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Breit Laboratories, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Breit Laboratories, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1985. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Breit Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Breit Laboratories, Inc.
5 devices
Cleared
Apr 25, 1985
IGM RHEUMATOID FACTOR TEST KIT
Immunology
37d
Cleared
Sep 05, 1984
COLOTRAK OCCULT BLOOD TEST
Hematology
211d
Cleared
Sep 05, 1984
OCCULT BLOOD TEST
Hematology
98d
Cleared
Aug 11, 1983
ANTI-N DNA ANTIBODY TEST KIT
Immunology
49d
Cleared
Jul 18, 1983
ANTINUCLEAR ANTIBODY TEST KIT
Immunology
33d