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WAVELENGTH MULTI-PURPOSE ULTRASOUND GEL

K012522 Class II Traditional
Decision Date
2001-10-18
Sponsor / Applicant
National Therapy Products, Inc.

Technical Specification

510(k) Submission ID K012522
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2001-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WAVELENGTH MULTI-PURPOSE ULTRASOUND GEL received FDA 510(k) clearance under submission number K012522, 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 2001-10-18.

Classification & Regulation

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