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FDA 510(k)

ADD-A-VIAL

K-Number: K904855 · 1990-11-19

ApplicantKendall Mcgaw Laboratories, Inc.
Decision Date1990-11-19
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADD-A-VIAL is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Mcgaw Laboratories, Inc.. It received FDA 510(k) clearance on 1990-11-19 under 510(k) number K904855. 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 ADD-A-VIAL?

ADD-A-VIAL is a medical device that received FDA 510(k) clearance on 1990-11-19. The listed applicant is Kendall Mcgaw Laboratories, Inc.. The 510(k) number is K904855.

When did ADD-A-VIAL receive FDA 510(k) clearance?

ADD-A-VIAL received FDA 510(k) clearance on 1990-11-19, under 510(k) number K904855.

Who is the listed applicant for ADD-A-VIAL?

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

What is the FDA product code for ADD-A-VIAL?

The FDA product code for ADD-A-VIAL is LHI.

Other records listing Kendall Mcgaw Laboratories, 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.

K905611MICRORATE PLUS INTELLIGENT PUMPK905610MICRORATE INTELLIGENT PUMPK904518VOLUMETRIC INFUSION PUMPK903809PROTECTED NEEDLE WITH OR WITHOUT IV SETK901065INFUSION PUMPK900865ADD-A-VIAL II BINARY CONNECTOR

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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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