Grifols USA, LLC
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113377 | GLIADIN IGA AND GLIADIN LGA | MST | 2012-12-14 | View |
| 510(k) | K120169 | INTERLAB IFE TEST USING G 26 VER. 2.0 INSTRUMENT | CFF | 2012-08-24 | View |
No matching devices.
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