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MULTI-CHANNEL DISCRETE ANALYZER (MDA-180)

K924453 Class II Traditional
Decision Date
1992-12-18
Sponsor / Applicant
Organon Teknika Corp.

Technical Specification

510(k) Submission ID K924453
Product Code JPA
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 1992-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) received FDA 510(k) clearance under submission number K924453, sponsored by Organon Teknika Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1992-12-18.

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.