meddevicedb.com FDA Device Reference

Iconic Latex Glove

K221648 Class I Traditional
Decision Date
2022-08-25
Sponsor / Applicant
Iconic Medicare Sdn Bhd

Technical Specification

510(k) Submission ID K221648
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2022-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Iconic Latex Glove received FDA 510(k) clearance under submission number K221648, sponsored by Iconic Medicare Sdn Bhd. 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 2022-08-25.

Classification & Regulation

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