meddevicedb.com FDA Device Reference

SYSTEMATE ALBUMIN

K843108 Class II Traditional
Decision Date
1984-08-27
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K843108
Product Code CIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1035
Decision Date 1984-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEMATE ALBUMIN received FDA 510(k) clearance under submission number K843108, sponsored by Em Diagnostic Systems, Inc.. 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 1984-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code CIX and 21 CFR 862.1035, within the Clinical Chemistry review panel as a Class II device.