meddevicedb.com FDA Device Reference

GLUCOSE OXIDASE REAGENT KIT

K800070 Class II Traditional
Decision Date
1980-02-05
Sponsor / Applicant
Fisher Scientific Co., LLC

Technical Specification

510(k) Submission ID K800070
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1980-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLUCOSE OXIDASE REAGENT KIT received FDA 510(k) clearance under submission number K800070, sponsored by Fisher Scientific Co., LLC. 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 1980-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.