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FDA 510(k)

LUER LOCK TRANSFER PIN

K-Number: K901063 · 1990-07-06

ApplicantAcacia, Inc.
Decision Date1990-07-06
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUER LOCK TRANSFER PIN is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 1990-07-06 under 510(k) number K901063. 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 LUER LOCK TRANSFER PIN?

LUER LOCK TRANSFER PIN is a medical device that received FDA 510(k) clearance on 1990-07-06. The listed applicant is Acacia, Inc.. The 510(k) number is K901063.

When did LUER LOCK TRANSFER PIN receive FDA 510(k) clearance?

LUER LOCK TRANSFER PIN received FDA 510(k) clearance on 1990-07-06, under 510(k) number K901063.

Who is the listed applicant for LUER LOCK TRANSFER PIN?

The FDA 510(k) record lists Acacia, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUER LOCK TRANSFER PIN?

The FDA product code for LUER LOCK TRANSFER PIN is LHI.

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Other records listing Acacia, Inc. 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.

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Related Devices (Code: LHI)

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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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