meddevicedb.com FDA Device Reference

MEDAC SYSTEM/3

K914925 Class II Traditional
Decision Date
1993-10-21
Sponsor / Applicant
Davicon, Inc.

Technical Specification

510(k) Submission ID K914925
Product Code HCC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5050
Decision Date 1993-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDAC SYSTEM/3 received FDA 510(k) clearance under submission number K914925, sponsored by Davicon, 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 1993-10-21.

Classification & Regulation

This clearance is catalogued under FDA product code HCC and 21 CFR 882.5050, within the Neurology review panel as a Class II device.