meddevicedb.com FDA Device Reference

OLYMPUS RF LATEX CALIBRATOR, AND OLYMPUS RF LATEX REAGENT WITH MODEL(S): ODC0028, AND OSR61105.

K060201 Class II Traditional
Decision Date
2006-06-06
Sponsor / Applicant
Olympus America, Inc.

Technical Specification

510(k) Submission ID K060201
Product Code DHR
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5775
Decision Date 2006-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS RF LATEX CALIBRATOR, AND OLYMPUS RF LATEX REAGENT WITH MODEL(S): ODC0028, AND OSR61105. received FDA 510(k) clearance under submission number K060201, 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 2006-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code DHR and 21 CFR 866.5775, within the Immunology review panel as a Class II device.