meddevicedb.com FDA Device Reference

IONOPHORELIC SWEAT STIM. CHLORIDE-

K832059 Class II Traditional
Decision Date
1983-08-24
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K832059
Product Code KTB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5525
Decision Date 1983-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IONOPHORELIC SWEAT STIM. CHLORIDE- received FDA 510(k) clearance under submission number K832059, 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 1983-08-24.

Classification & Regulation

This clearance is catalogued under FDA product code KTB and 21 CFR 890.5525, within the Physical Medicine review panel as a Class II device.