meddevicedb.com FDA Device Reference

CDS 3-PD HEMATOLOGY CONTROLS

K024173 Class II Traditional
Decision Date
2003-01-14
Sponsor / Applicant
Clinical Diagnostic Solutions, Inc.

Technical Specification

510(k) Submission ID K024173
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2003-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CDS 3-PD HEMATOLOGY CONTROLS received FDA 510(k) clearance under submission number K024173, sponsored by Clinical Diagnostic Solutions, 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 2003-01-14.

Classification & Regulation

This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.