meddevicedb.com FDA Device Reference

SHARPS CONTAINER

K110262 Class II Traditional
Decision Date
2011-04-05
Sponsor / Applicant
Noble Marketing

Technical Specification

510(k) Submission ID K110262
Product Code MMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2011-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHARPS CONTAINER received FDA 510(k) clearance under submission number K110262, sponsored by Noble Marketing. 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 2011-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code MMK and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.