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ELECTRA 1800C AUTOMATIC COAGULATION ANALYZER

K962664 Class II Traditional
Decision Date
1996-09-10
Sponsor / Applicant
Medical Laboratory Automation Systems, Inc.

Technical Specification

510(k) Submission ID K962664
Product Code GKP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1996-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRA 1800C AUTOMATIC COAGULATION ANALYZER received FDA 510(k) clearance under submission number K962664, 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 1996-09-10.

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.