meddevicedb.com FDA Device Reference

AMRESCO CREATININE REAGENT #4316100

K896686 Class II Traditional
Decision Date
1990-02-08
Sponsor / Applicant
American Research Products Co.

Technical Specification

510(k) Submission ID K896686
Product Code CGX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 1990-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMRESCO CREATININE REAGENT #4316100 received FDA 510(k) clearance under submission number K896686, sponsored by American Research Products Co.. 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 1990-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code CGX and 21 CFR 862.1225, within the Clinical Chemistry review panel as a Class II device.