meddevicedb.com FDA Device Reference

ELECTRA 1400C AUTOMATIC COAGULATION ANALYZER

K944227 Class II Traditional
Decision Date
1995-02-03
Sponsor / Applicant
Medical Laboratory Automation Systems, Inc.

Technical Specification

510(k) Submission ID K944227
Product Code GKP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1995-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRA 1400C AUTOMATIC COAGULATION ANALYZER received FDA 510(k) clearance under submission number K944227, sponsored by Medical Laboratory Automation Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1995-02-03.

Classification & Regulation

This clearance is catalogued under FDA product code GKP and 21 CFR 864.5400, within the Hematology review panel as a Class II device.