meddevicedb.com FDA Device Reference

Nitrile Examination Gloves

K212929 Class I Traditional
Decision Date
2022-04-09
Sponsor / Applicant
Watchtower Ppe Supplies, Inc.

Technical Specification

510(k) Submission ID K212929
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2022-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nitrile Examination Gloves received FDA 510(k) clearance under submission number K212929, sponsored by Watchtower Ppe Supplies, 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 2022-04-09.

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.