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SONIC-STIM

K063135 Class II Traditional
Decision Date
2007-02-05
Sponsor / Applicant
Naimco, Inc.

Technical Specification

510(k) Submission ID K063135
Product Code IMG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5860
Decision Date 2007-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONIC-STIM received FDA 510(k) clearance under submission number K063135, sponsored by Naimco, Inc.. 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 2007-02-05.

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.