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CLICKFINE PEN NEEDLE

K100436 Class II Special
Decision Date
2010-04-30
Sponsor / Applicant
Ypsomed AG

Technical Specification

510(k) Submission ID K100436
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2010-04-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLICKFINE PEN NEEDLE received FDA 510(k) clearance under submission number K100436, sponsored by Ypsomed AG. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2010-04-30.

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.