meddevicedb.com FDA Device Reference

TECHNICON SMA & AAII SYSTEMS

K770406 Class II Traditional
Decision Date
1977-06-02
Sponsor / Applicant
Boehringer Laboratories

Technical Specification

510(k) Submission ID K770406
Product Code CJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1050
Decision Date 1977-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TECHNICON SMA & AAII SYSTEMS received FDA 510(k) clearance under submission number K770406, sponsored by Boehringer Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1977-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code CJE and 21 CFR 862.1050, within the Clinical Chemistry review panel as a Class II device.