Euroimmun Us, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Euroimmun Us, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Euroimmun Us, LLC has 6 FDA 510(k) cleared medical devices. Based in Boonton Twp, US.
Historical record: 6 cleared submissions from 2006 to 2007. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Euroimmun Us, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Euroimmun Us, LLC
6 devices
Cleared
Dec 31, 2007
EUROIMMUN ANTI-CCP ELISA
Immunology
284d
Cleared
Jun 28, 2007
EUROIMMUN ANTI-HSV-2 ELISA (IGG) AND ANTI-HSV-1 ELISA (IGG) KIT
Microbiology
421d
Cleared
May 22, 2007
EUROIMMUN ANA IFA: HEP-20-10
Immunology
63d
Cleared
Oct 05, 2006
EUROIMMUN ENDOMYSIUM IFA: ESOPHAGUS (MONKEY) KIT
Immunology
136d
Cleared
Sep 08, 2006
EUROIMMUN PR3 ELISA KIT. EUROIMMUN MPO ELISA KIT.
Immunology
177d
Cleared
Feb 16, 2006
EUROIMMUN ANCA IFA GRANULOCYTE BIOCHIP MOSCAIC IGG ANTIBODY IN HUMAN SERUM
Immunology
255d