Company ยท ES
Laboratorios Grifols, S.A.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2017. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 19, 2017 | K162216 | GRI-FILL PERISTALTIC SET Laboratorios Grifols, S.A., ES | LHI |
| Jan 13, 2011 | K102590 | FLEBOSET DOUBLE Laboratorios Grifols, S.A., ES | LHI |
| Jan 27, 2010 | K093182 | SET GRI-FILL 3.0 Laboratorios Grifols, S.A., ES | LHI |
| Sep 29, 2008 | K082752 | QUICKPIN Laboratorios Grifols, S.A., ES | LHI |
| Feb 25, 2005 | K050339 | SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE Laboratorios Grifols, S.A., ES | LHI |
| Mar 9, 2004 | K040456 | FLEBOSET MULTIPLE Laboratorios Grifols, S.A., ES | LHI |
| Dec 30, 2003 | K033916 | GRI-BAG, GRI-BAG AP Laboratorios Grifols, S.A., ES | KPE |
| Dec 17, 2003 | K033682 | SET GRI-FILL 2.0-1 WAY; 2.0-2 WAYS; LUER CONNECTION TUBE Laboratorios Grifols, S.A., ES | LHI |
| Nov 24, 2003 | K031419 | GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML Laboratorios Grifols, S.A., ES | KPE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||