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

K120661 Class II Traditional
Decision Date
2012-06-03
Sponsor / Applicant
Vidacare Corporation

Technical Specification

510(k) Submission ID K120661
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2012-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE received FDA 510(k) clearance under submission number K120661, sponsored by Vidacare Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2012-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.