Biokit, S.A. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Biokit, S.A. has 23 FDA 510(k) cleared medical devices. Based in Barcelona, ES.
Latest FDA clearance: Feb 2025. Active since 2005.
Browse the FDA 510(k) cleared devices submitted by Biokit, S.A. Filter by specialty or product code using the sidebar.
23 devices
Cleared
Feb 12, 2025
ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG...
Microbiology
85d
Cleared
Aug 07, 2024
ADVIA Centaur EBV-EBNA IgG
Microbiology
272d
Cleared
Aug 07, 2024
ADVIA Centaur EBV-VCA IgM
Microbiology
272d
Cleared
Sep 20, 2023
ARCHITECT HSV-1 IgG, ARCHITECT HSV-1 IgG Calibrator, ARCHITECT HSV-1 IgG...
Microbiology
639d
Cleared
Feb 21, 2023
Quantia IgE
Immunology
421d
Cleared
Aug 23, 2018
ADVIA Centaur Herpes-1 IgG
Microbiology
94d
Cleared
Aug 23, 2018
ADVIA Centaur Herpes-2 IgG
Microbiology
94d
Cleared
Feb 11, 2016
ARCHITECT SHBG
Chemistry
190d
Cleared
Dec 19, 2013
LP(A) CALIBRATORS, AND LP(A) CONTROLS
Chemistry
140d
Cleared
Aug 29, 2013
ARCHITECT IVANCOMYCIN
Toxicology
251d
Cleared
Nov 23, 2011
ARCHITECT 25-OH VITAMIN D 100T, VITAMIN D 500T, VITAMIN D CALIBRATORS,...
Chemistry
265d
Cleared
Dec 22, 2008
ARCHITECT IDIGOXIN AND ARCHITECT IDIGOXIN CALIBRATORS, MODELS 1P32-25 AND...
Toxicology
80d