meddevicedb.com FDA Device Reference

HI CHEM CO2 ALKALINE BUFFER REAGENT KIT,PROD#88813

K925553 Class II Traditional
Decision Date
1993-02-12
Sponsor / Applicant
Hichem Diagnostics

Technical Specification

510(k) Submission ID K925553
Product Code JFL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 1993-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HI CHEM CO2 ALKALINE BUFFER REAGENT KIT,PROD#88813 received FDA 510(k) clearance under submission number K925553, sponsored by Hichem Diagnostics. 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 1993-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code JFL and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.