meddevicedb.com FDA Device Reference

OAK RIDGE PRODUCTS MULTI-PURPOSE SHARPS CONTAINERS

K141759 Class II Traditional
Decision Date
2014-10-24
Sponsor / Applicant
Oak Ridge Products, LLC

Technical Specification

510(k) Submission ID K141759
Product Code MMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2014-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OAK RIDGE PRODUCTS MULTI-PURPOSE SHARPS CONTAINERS received FDA 510(k) clearance under submission number K141759, sponsored by Oak Ridge Products, LLC. 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 2014-10-24.

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.