meddevicedb.com FDA Device Reference

BODY SYSTEM

K942223 Class I Traditional
Decision Date
1994-06-09
Sponsor / Applicant
Conair Corp.

Technical Specification

510(k) Submission ID K942223
Product Code ISA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1994-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BODY SYSTEM received FDA 510(k) clearance under submission number K942223, sponsored by Conair Corp.. 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 1994-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code ISA and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.