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FDA 510(k)

MAGUN BASE I.V. POLE

K-Number: K821405 · 1982-06-16

ApplicantManuco Manufacturing Co., Inc.
Decision Date1982-06-16
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAGUN BASE I.V. POLE is the device name listed in this FDA 510(k) record. The listed applicant is Manuco Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1982-06-16 under 510(k) number K821405. 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 MAGUN BASE I.V. POLE?

MAGUN BASE I.V. POLE is a medical device that received FDA 510(k) clearance on 1982-06-16. The listed applicant is Manuco Manufacturing Co., Inc.. The 510(k) number is K821405.

When did MAGUN BASE I.V. POLE receive FDA 510(k) clearance?

MAGUN BASE I.V. POLE received FDA 510(k) clearance on 1982-06-16, under 510(k) number K821405.

Who is the listed applicant for MAGUN BASE I.V. POLE?

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

What is the FDA product code for MAGUN BASE I.V. POLE?

The FDA product code for MAGUN BASE I.V. POLE is FOX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Manuco Manufacturing Co., 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.

K821403LIGHT WEIGHT ALUMINUM CRUTCHESK821404LIGHT WEIGHT ALUMINUM WALKERK821402LIGHT WEIGHT ALUMINUM CANES

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

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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