meddevicedb.com FDA Device Reference

ATM Glove

K213016 Class I Traditional
Decision Date
2021-12-28
Sponsor / Applicant
Phu Duc Huy Production Trading Services Corporation

Technical Specification

510(k) Submission ID K213016
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2021-12-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATM Glove received FDA 510(k) clearance under submission number K213016, sponsored by Phu Duc Huy Production Trading Services Corporation. 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 2021-12-28.

Classification & Regulation

This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.