meddevicedb.com FDA Device Reference

OTE BIOMEDICAL #1296 - 16 CHAN. RECORD

K820779 Class II Traditional
Decision Date
1982-04-26
Sponsor / Applicant
Del Mar Avionics

Technical Specification

510(k) Submission ID K820779
Product Code GWQ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 1982-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OTE BIOMEDICAL #1296 - 16 CHAN. RECORD received FDA 510(k) clearance under submission number K820779, sponsored by Del Mar Avionics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1982-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code GWQ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.