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SHARPS CONTAINER

K101567 Class II Traditional
Decision Date
2010-09-02
Sponsor / Applicant
Cixi Leinuo Plastic Co., Ltd.

Technical Specification

510(k) Submission ID K101567
Product Code MMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 2010-09-02
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 K101567, sponsored by Cixi Leinuo Plastic Co., Ltd.. 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 2010-09-02.

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.