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FDA 510(k)

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

K-Number: K050339 · 2005-02-25

ApplicantLaboratorios Grifols, S.A.
Decision Date2005-02-25
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is Laboratorios Grifols, S.A.. It received FDA 510(k) clearance on 2005-02-25 under 510(k) number K050339. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE?

SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE is a medical device that received FDA 510(k) clearance on 2005-02-25. The listed applicant is Laboratorios Grifols, S.A.. The 510(k) number is K050339.

When did SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE receive FDA 510(k) clearance?

SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE received FDA 510(k) clearance on 2005-02-25, under 510(k) number K050339.

Who is the listed applicant for SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE?

The FDA 510(k) record lists Laboratorios Grifols, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE?

The FDA product code for SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE is LHI.

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Other records listing Laboratorios Grifols, S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K162216GRI-FILL PERISTALTIC SETK102590FLEBOSET DOUBLEK093182SET GRI-FILL 3.0K082752QUICKPINK040456FLEBOSET MULTIPLEK033916GRI-BAG, GRI-BAG AP

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Related Devices (Code: LHI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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