meddevicedb.com FDA Device Reference

NEUROMUSCULAR ELECTRICAL STIMULATOR

K940349 Class II Traditional
Decision Date
1994-04-01
Sponsor / Applicant
Progressive Concepts, Inc.

Technical Specification

510(k) Submission ID K940349
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1994-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROMUSCULAR ELECTRICAL STIMULATOR received FDA 510(k) clearance under submission number K940349, sponsored by Progressive Concepts, 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 1994-04-01.

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.