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FDA 510(k)

QUICKPIN

K-Number: K082752 · 2008-09-29

ApplicantLaboratorios Grifols, S.A.
Decision Date2008-09-29
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUICKPIN 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 2008-09-29 under 510(k) number K082752. 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 QUICKPIN?

QUICKPIN is a medical device that received FDA 510(k) clearance on 2008-09-29. The listed applicant is Laboratorios Grifols, S.A.. The 510(k) number is K082752.

When did QUICKPIN receive FDA 510(k) clearance?

QUICKPIN received FDA 510(k) clearance on 2008-09-29, under 510(k) number K082752.

Who is the listed applicant for QUICKPIN?

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 QUICKPIN?

The FDA product code for QUICKPIN is LHI.

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

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K162216GRI-FILL PERISTALTIC SETK102590FLEBOSET DOUBLEK093182SET GRI-FILL 3.0K050339SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLEK040456FLEBOSET 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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