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FDA 510(k)

IV POLE/STAND

K-Number: K952196 · 1995-07-31

ApplicantValentine Intl. , Ltd.
Decision Date1995-07-31
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV POLE/STAND is the device name listed in this FDA 510(k) record. The listed applicant is Valentine Intl. , Ltd.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K952196. 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 IV POLE/STAND?

IV POLE/STAND is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Valentine Intl. , Ltd.. The 510(k) number is K952196.

When did IV POLE/STAND receive FDA 510(k) clearance?

IV POLE/STAND received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952196.

Who is the listed applicant for IV POLE/STAND?

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

What is the FDA product code for IV POLE/STAND?

The FDA product code for IV POLE/STAND 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.K950367IV SHUTTLEEquipment Concepts, Inc.K946201STAND, INFUSIONMedical Specialties, 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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