Medical Device Manufacturer · ES , Parets Del Valles, Barcelona

Laboratorios Grifols, S.A. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2003

Total

Cleared

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.

FDA 510(k) Regulatory Record - Laboratorios Grifols, S.A.

9 devices

1-9 of 9

Cleared Oct 19, 2017

GRI-FILL PERISTALTIC SET

K162216 · LHI

General Hospital · 437d

Cleared Jan 13, 2011

FLEBOSET DOUBLE

K102590 · LHI

General Hospital · 126d

Cleared Jan 27, 2010

SET GRI-FILL 3.0

K093182 · LHI

General Hospital · 111d

Cleared Sep 29, 2008

QUICKPIN

K082752 · LHI

General Hospital · 10d

Cleared Feb 25, 2005

SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE

K050339 · LHI

General Hospital · 14d

Cleared Mar 09, 2004

FLEBOSET MULTIPLE

K040456 · LHI

General Hospital · 15d

Cleared Dec 30, 2003

GRI-BAG, GRI-BAG AP

K033916 · KPE

General Hospital · 12d

Cleared Dec 17, 2003

SET GRI-FILL 2.0-1 WAY

K033682 · LHI

General Hospital · 23d

Cleared Nov 24, 2003

GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML

K031419 · KPE

General Hospital · 203d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026

Laboratorios Grifols, S.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Laboratorios Grifols, S.A.

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