meddevicedb.com FDA Device Reference

MemorialTM Gloves

K231740 Class I Traditional
Decision Date
2023-07-04
Sponsor / Applicant
Us Glove Supply

Technical Specification

510(k) Submission ID K231740
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2023-07-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MemorialTM Gloves received FDA 510(k) clearance under submission number K231740, sponsored by Us Glove Supply. 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 2023-07-04.

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.