meddevicedb.com FDA Device Reference

AUTO SECTOR MCU

K813596 Class II Traditional
Decision Date
1982-03-25
Sponsor / Applicant
Technicare Corp.

Technical Specification

510(k) Submission ID K813596
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1982-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SECTOR MCU received FDA 510(k) clearance under submission number K813596, sponsored by Technicare Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1982-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.