meddevicedb.com FDA Device Reference

UltiCare Disposable Pen Needles

K213407 Class II Traditional
Decision Date
2021-12-16
Sponsor / Applicant
Ultimed Incorporated

Technical Specification

510(k) Submission ID K213407
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2021-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UltiCare Disposable Pen Needles received FDA 510(k) clearance under submission number K213407, sponsored by Ultimed Incorporated. 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 2021-12-16.

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.