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FDA 510(k)

INTERLINK UNIVERSAL VIAL ADAPTER

K-Number: K924064 · 1993-04-21

ApplicantBaxter Healthcare Corp
Decision Date1993-04-21
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTERLINK UNIVERSAL VIAL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1993-04-21 under 510(k) number K924064. 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 INTERLINK UNIVERSAL VIAL ADAPTER?

INTERLINK UNIVERSAL VIAL ADAPTER is a medical device that received FDA 510(k) clearance on 1993-04-21. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K924064.

When did INTERLINK UNIVERSAL VIAL ADAPTER receive FDA 510(k) clearance?

INTERLINK UNIVERSAL VIAL ADAPTER received FDA 510(k) clearance on 1993-04-21, under 510(k) number K924064.

Who is the listed applicant for INTERLINK UNIVERSAL VIAL ADAPTER?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERLINK UNIVERSAL VIAL ADAPTER?

The FDA product code for INTERLINK UNIVERSAL VIAL ADAPTER is LHI.

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Other records listing Baxter Healthcare Corp 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.

K190910PrisMax System Version 2K163530PrisMax Control UnitK132734NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETSK130245LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFOK123874INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL SK123868INTERLINK SYSTEM LEVER LOCK CANNULA WITH CHECK VALVE, SECONDARY MEDICATION SETS, SOLUTION SETS, CONTINU-FLO SOLUTION SET

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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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