Laboratorios Grifols, S.A. is one of 87 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Laboratorios Grifols, S.A. - FDA 510(k) Cleared Devices
Recent clearances: GRI-FILL PERISTALTIC SET, FLEBOSET DOUBLE, SET GRI-FILL 3.0
9
Total
9
Cleared
0
Denied
Laboratorios Grifols, S.A. has 9 FDA 510(k) cleared medical devices. Based in Parets Del Valles, Barcelona, ES.
Historical record: 9 cleared submissions from 2003 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Laboratorios Grifols, S.A. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Tuv Sud America, Inc..
FDA 510(k) Regulatory Record - Laboratorios Grifols, S.A.
9 devices
Cleared
Oct 19, 2017
GRI-FILL PERISTALTIC SET
General Hospital
437d
Cleared
Jan 13, 2011
FLEBOSET DOUBLE
General Hospital
126d
Cleared
Jan 27, 2010
SET GRI-FILL 3.0
General Hospital
111d
Cleared
Sep 29, 2008
QUICKPIN
General Hospital
10d
Cleared
Feb 25, 2005
SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE
General Hospital
14d
Cleared
Mar 09, 2004
FLEBOSET MULTIPLE
General Hospital
15d
Cleared
Dec 30, 2003
GRI-BAG, GRI-BAG AP
General Hospital
12d
Cleared
Dec 17, 2003
SET GRI-FILL 2.0-1 WAY
General Hospital
23d
Cleared
Nov 24, 2003
GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML
General Hospital
203d