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NEUROMUSCULAR STIMULATOR 3105

K840467 Class II Traditional
Decision Date
1984-02-17
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K840467
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1984-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROMUSCULAR STIMULATOR 3105 received FDA 510(k) clearance under submission number K840467, sponsored by Medtronic Vascular. 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 1984-02-17.

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.