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ACCOUSONIC, MODEL AS-270

K030878 Class II Special
Decision Date
2003-03-28
Sponsor / Applicant
Metron Medical Australia, Pty, Ltd.

Technical Specification

510(k) Submission ID K030878
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 2003-03-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCOUSONIC, MODEL AS-270 received FDA 510(k) clearance under submission number K030878, sponsored by Metron Medical Australia, Pty, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2003-03-28.

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.