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SONICATOR 720 (MODEL ME720)

K883228 Class II Traditional
Decision Date
1988-08-18
Sponsor / Applicant
Mettler Electronics Corp.

Technical Specification

510(k) Submission ID K883228
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 1988-08-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONICATOR 720 (MODEL ME720) received FDA 510(k) clearance under submission number K883228, sponsored by Mettler Electronics Corp.. 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 1988-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.