meddevicedb.com FDA Device Reference

OLYMPUS ASPARTATE AMINOTRANSFERASE REAGENT

K925155 Class II Traditional
Decision Date
1993-01-26
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K925155
Product Code CIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1100
Decision Date 1993-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS ASPARTATE AMINOTRANSFERASE REAGENT received FDA 510(k) clearance under submission number K925155, sponsored by Olympus Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1993-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code CIT and 21 CFR 862.1100, within the Clinical Chemistry review panel as a Class II device.