Grifols USA, LLC is one of 5344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grifols USA, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Grifols USA, LLC has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Grifols USA, LLC Filter by specialty or product code using the sidebar.
Grifols USA, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 14, 2012
GLIADIN IGA AND GLIADIN LGA
Immunology
394d
Cleared
Aug 24, 2012
INTERLAB IFE TEST USING G 26 VER. 2.0 INSTRUMENT
Immunology
218d