meddevicedb.com FDA Device Reference

JSM Insulin Pen Needle

K152166 Class II Traditional
Decision Date
2016-07-11
Sponsor / Applicant
Jeesung Medical Co., Ltd.

Technical Specification

510(k) Submission ID K152166
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2016-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JSM Insulin Pen Needle received FDA 510(k) clearance under submission number K152166, sponsored by Jeesung Medical Co., Ltd.. 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 2016-07-11.

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.