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IMC HYPODERMIC NEEDLE

K102584 Class II Traditional
Decision Date
2011-01-14
Sponsor / Applicant
International Medsurg Connection

Technical Specification

510(k) Submission ID K102584
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2011-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMC HYPODERMIC NEEDLE received FDA 510(k) clearance under submission number K102584, sponsored by International Medsurg Connection. 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 2011-01-14.

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.