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ELECTRA 1000C AUTOMATIC COAGULATION TIMER

K894052 Class II Traditional
Decision Date
1989-07-27
Sponsor / Applicant
Medical Laboratory Automation Systems, Inc.

Technical Specification

510(k) Submission ID K894052
Product Code GKP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1989-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRA 1000C AUTOMATIC COAGULATION TIMER received FDA 510(k) clearance under submission number K894052, 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 1989-07-27.

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.