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POLYSONIC ULTRASOUND LOTION

K827296 Class II Traditional
Decision Date
1982-04-16
Sponsor / Applicant
Parker Laboratories, Inc.

Technical Specification

510(k) Submission ID K827296
Product Code MUI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 1982-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYSONIC ULTRASOUND LOTION received FDA 510(k) clearance under submission number K827296, sponsored by Parker Laboratories, 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 1982-04-16.

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.