Diagnostic Grifols, S.A. is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Diagnostic Grifols, S.A. - FDA 510(k) Cleared Devices
Recent clearances: QNext and DG-PT
1
Total
1
Cleared
0
Denied
Diagnostic Grifols, S.A. has 1 FDA 510(k) cleared medical devices. Based in Partes Del Valles, ES.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Diagnostic Grifols, S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostic Grifols, S.A.
1 devices