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SONICATOR PLUS 940, MODEL ME940

K071137 Class II Abbreviated
Decision Date
2007-08-01
Sponsor / Applicant
Mettler Electronics Corp.

Technical Specification

510(k) Submission ID K071137
Product Code IMG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5860
Decision Date 2007-08-01
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONICATOR PLUS 940, MODEL ME940 received FDA 510(k) clearance under submission number K071137, sponsored by Mettler Electronics Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2007-08-01.

Classification & Regulation

This clearance is catalogued under FDA product code IMG and 21 CFR 890.5860, within the Physical Medicine review panel as a Class II device.