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CLEANE / CLEANE POP

K111341 Class II Traditional
Decision Date
2012-02-29
Sponsor / Applicant
Medicon Co., Ltd.

Technical Specification

510(k) Submission ID K111341
Product Code OZC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5740
Decision Date 2012-02-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEANE / CLEANE POP received FDA 510(k) clearance under submission number K111341, sponsored by Medicon Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2012-02-29.

Classification & Regulation

This clearance is catalogued under FDA product code OZC and 21 CFR 890.5740, within the Physical Medicine review panel as a Class II device.