meddevicedb.com FDA Device Reference

Safety Pen Needle

K210864 Class II Traditional
Decision Date
2022-02-17
Sponsor / Applicant
Sandstone Medical (Suzhou), Inc.

Technical Specification

510(k) Submission ID K210864
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2022-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Safety Pen Needle received FDA 510(k) clearance under submission number K210864, sponsored by Sandstone Medical (Suzhou), Inc.. 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 2022-02-17.

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.