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FDA 510(k)

VITALMIX (SET & BAG)

K-Number: K902482 · 1990-07-02

ApplicantPacific Device, Inc.
Decision Date1990-07-02
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITALMIX (SET & BAG) is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Device, Inc.. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K902482. 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 VITALMIX (SET & BAG)?

VITALMIX (SET & BAG) is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Pacific Device, Inc.. The 510(k) number is K902482.

When did VITALMIX (SET & BAG) receive FDA 510(k) clearance?

VITALMIX (SET & BAG) received FDA 510(k) clearance on 1990-07-02, under 510(k) number K902482.

Who is the listed applicant for VITALMIX (SET & BAG)?

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

What is the FDA product code for VITALMIX (SET & BAG)?

The FDA product code for VITALMIX (SET & BAG) is LHI.

Related Clinical Trials

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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Other records listing Pacific Device, 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.

K972464VITALMIX PLUS EMPTY I.V. CONTAINERK923782TRANSFER SETK912860INTRAVASCULAR ADMINISTRATION SETSK912596MECONIUM ASPIRATION

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

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

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