meddevicedb.com FDA Device Reference

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.

K801577 Class II Traditional
Decision Date
1980-08-27
Sponsor / Applicant
Inter Med Industries, Inc.

Technical Specification

510(k) Submission ID K801577
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1980-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. received FDA 510(k) clearance under submission number K801577, sponsored by Inter Med Industries, 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 1980-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.