meddevicedb.com FDA Device Reference

Safety Winged Blood Collection Sets

K211293 Class II Traditional
Decision Date
2021-06-25
Sponsor / Applicant
Promisemed Hangzhou Meditech Co., Ltd.

Technical Specification

510(k) Submission ID K211293
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2021-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Safety Winged Blood Collection Sets received FDA 510(k) clearance under submission number K211293, sponsored by Promisemed Hangzhou Meditech 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 2021-06-25.

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.