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FDA 510(k)

THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE

K-Number: K120661 · 2012-06-03

ApplicantVidacare Corporation
Decision Date2012-06-03
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE is the device name listed in this FDA 510(k) record. The listed applicant is Vidacare Corporation. It received FDA 510(k) clearance on 2012-06-03 under 510(k) number K120661. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE?

THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE is a medical device that received FDA 510(k) clearance on 2012-06-03. The listed applicant is Vidacare Corporation. The 510(k) number is K120661.

When did THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE receive FDA 510(k) clearance?

THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE received FDA 510(k) clearance on 2012-06-03, under 510(k) number K120661.

Who is the listed applicant for THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE?

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 THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE?

The FDA product code for THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE is FMI.

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Other records listing Vidacare Corporation as applicant

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Related Devices (Code: FMI)

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.

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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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