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FDA 510(k)

AIV SYSTEMS' IV POLES

K-Number: K895776 · 1990-02-28

ApplicantAutomated IV Systems, Inc.
Decision Date1990-02-28
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AIV SYSTEMS' IV POLES is the device name listed in this FDA 510(k) record. The listed applicant is Automated IV Systems, Inc.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K895776. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIV SYSTEMS' IV POLES?

AIV SYSTEMS' IV POLES is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Automated IV Systems, Inc.. The 510(k) number is K895776.

When did AIV SYSTEMS' IV POLES receive FDA 510(k) clearance?

AIV SYSTEMS' IV POLES received FDA 510(k) clearance on 1990-02-28, under 510(k) number K895776.

Who is the listed applicant for AIV SYSTEMS' IV POLES?

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

What is the FDA product code for AIV SYSTEMS' IV POLES?

The FDA product code for AIV SYSTEMS' IV POLES is FOX.

Related Clinical Trials

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Related Devices (Code: FOX)

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.

K980336IV STANDSClinton Industries, Inc.K964782MEDRAD CONTRAST HOLDERMedrad, Inc.K961470PORT-A-POLEPrins Medical Ind., Inc.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.K950367IV SHUTTLEEquipment Concepts, Inc.

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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