meddevicedb.com FDA Device Reference

HEMOGLOBIN ELECTROPHORESIS METH ON THE-

K831055 Class II Traditional
Decision Date
1983-06-08
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K831055
Product Code JBO
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7275
Decision Date 1983-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOGLOBIN ELECTROPHORESIS METH ON THE- received FDA 510(k) clearance under submission number K831055, sponsored by Olympus 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 1983-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code JBO and 21 CFR 864.7275, within the Hematology review panel as a Class II device.