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MODEL EM-2 BIOELECTRIC PROCESSOR

K830034 Class II Traditional
Decision Date
1983-02-09
Sponsor / Applicant
Myo-Tronics Research, Inc.

Technical Specification

510(k) Submission ID K830034
Product Code KZM
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1375
Decision Date 1983-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL EM-2 BIOELECTRIC PROCESSOR received FDA 510(k) clearance under submission number K830034, sponsored by Myo-Tronics Research, 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 1983-02-09.

Classification & Regulation

This clearance is catalogued under FDA product code KZM and 21 CFR 890.1375, within the Physical Medicine review panel as a Class II device.