FDA 510(k)

PORT-A-POLE

K-Number: K961470 · 1996-07-22

Decision Date1996-07-22

Product CodeFOX

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PORT-A-POLE is the device name listed in this FDA 510(k) record. The listed applicant is Prins Medical Ind., Inc.. It received FDA 510(k) clearance on 1996-07-22 under 510(k) number K961470. 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 PORT-A-POLE?

PORT-A-POLE is a medical device that received FDA 510(k) clearance on 1996-07-22. The listed applicant is Prins Medical Ind., Inc.. The 510(k) number is K961470.

When did PORT-A-POLE receive FDA 510(k) clearance?

PORT-A-POLE received FDA 510(k) clearance on 1996-07-22, under 510(k) number K961470.

Who is the listed applicant for PORT-A-POLE?

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

What is the FDA product code for PORT-A-POLE?

The FDA product code for PORT-A-POLE is FOX.

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.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.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.