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#ST10 PROGR. EVOKED RESPONSE STIMULATOR

K822744 Class II Traditional
Decision Date
1982-11-03
Sponsor / Applicant
Teca, Inc.

Technical Specification

510(k) Submission ID K822744
Product Code GWF
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1870
Decision Date 1982-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

#ST10 PROGR. EVOKED RESPONSE STIMULATOR received FDA 510(k) clearance under submission number K822744, sponsored by Teca, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1982-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.