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CLICKFINE AUTOPROTECT PEN NEEDLE

K131123 Class II Traditional
Decision Date
2013-07-05
Sponsor / Applicant
Ypsomed AG

Technical Specification

510(k) Submission ID K131123
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2013-07-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLICKFINE AUTOPROTECT PEN NEEDLE received FDA 510(k) clearance under submission number K131123, sponsored by Ypsomed AG. 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 2013-07-05.

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.