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WAVELENGHT ULTRASOUND LOTION

K013212 Class II Traditional
Decision Date
2002-02-25
Sponsor / Applicant
National Therapy Products, Inc.

Technical Specification

510(k) Submission ID K013212
Product Code MUI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2002-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WAVELENGHT ULTRASOUND LOTION received FDA 510(k) clearance under submission number K013212, sponsored by National Therapy Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code MUI and 21 CFR 892.1570, within the Radiology review panel as a Class II device.