meddevicedb.com FDA Device Reference

Promisemed Triple Safety Pen Needle

K202682 Class II Special
Decision Date
2020-11-24
Sponsor / Applicant
Promisemed Hangzhou Meditech Co., Ltd.

Technical Specification

510(k) Submission ID K202682
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2020-11-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Promisemed Triple Safety Pen Needle received FDA 510(k) clearance under submission number K202682, sponsored by Promisemed Hangzhou Meditech Co., Ltd.. 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 2020-11-24.

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.