meddevicedb.com FDA Device Reference

OLYMPUS CRP LATEX REAGENT, OSR6199; OLYMPUS CRP LATEX CALIBRATOR NORMAL SET, ODC0026; OLYMPUS CRP LATEX CALIBRATOR HIGH

K051564 Class II Traditional
Decision Date
2005-08-22
Sponsor / Applicant
Olympus America, Inc.

Technical Specification

510(k) Submission ID K051564
Product Code NQD
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2005-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS CRP LATEX REAGENT, OSR6199; OLYMPUS CRP LATEX CALIBRATOR NORMAL SET, ODC0026; OLYMPUS CRP LATEX CALIBRATOR HIGH received FDA 510(k) clearance under submission number K051564, sponsored by Olympus America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2005-08-22.

Classification & Regulation

This clearance is catalogued under FDA product code NQD and 21 CFR 866.5270, within the Immunology review panel as a Class II device.