meddevicedb.com FDA Device Reference

CBC-SF

K010409 Class II Traditional
Decision Date
2001-03-16
Sponsor / Applicant
R&D Systems, Inc.

Technical Specification

510(k) Submission ID K010409
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2001-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CBC-SF received FDA 510(k) clearance under submission number K010409, sponsored by R&D 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 2001-03-16.

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.