meddevicedb.com FDA Device Reference

MLA ELECTRA 750 COAGULATION TIMER

K780810 Class II Traditional
Decision Date
1978-06-14
Sponsor / Applicant
Medical Laboratory Automation Systems, Inc.

Technical Specification

510(k) Submission ID K780810
Product Code JPA
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 1978-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MLA ELECTRA 750 COAGULATION TIMER received FDA 510(k) clearance under submission number K780810, 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 1978-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code JPA and 21 CFR 864.5425, within the Hematology review panel as a Class II device.