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FDA 510(k)

POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM

K-Number: K062833 · 2006-11-30

ApplicantVidacare Corporation
Decision Date2006-11-30
Product CodeFCF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vidacare Corporation. It received FDA 510(k) clearance on 2006-11-30 under 510(k) number K062833. The device is classified under product code FCF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM?

POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM is a medical device that received FDA 510(k) clearance on 2006-11-30. The listed applicant is Vidacare Corporation. The 510(k) number is K062833.

When did POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM receive FDA 510(k) clearance?

POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM received FDA 510(k) clearance on 2006-11-30, under 510(k) number K062833.

Who is the listed applicant for POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM?

The FDA 510(k) record lists Vidacare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM?

The FDA product code for POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM is FCF.

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Other records listing Vidacare Corporation 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.

K120661THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACREK113872THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACAREK101026POWERED PD-IO INFUSION SYSTEM, EZ-IO HUMERAL HEAD, POWERED PH-IOK091140EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, EZ-IOK081713VERTEBRAL ACCESS SYSTEM BY VIDACAREK072045ONCONTROL BONE MARROW BIOPSY SYSTEM

View all 18 devices →

Related Devices (Code: FCF)

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.

K070759POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEMVidacare CorporationK984168BARRETT'S ESOPHAGEAL CYTOLOGY DEVICEUnited States Endoscopy Group, Inc.K915142AMCATH DISPOSABLE BIOPSY FORCEPSIntl. Medical, Inc.K911155OVAL CUP BIOPSY FORCEPEndovationsK843477PHARMA-PLAST RECTAL TIPZimmar Consulting , Ltd.

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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