meddevicedb.com FDA Device Reference

ACE AXCEL CLINICAL CHEMISTRY SYSTEM,ACE ALBUMIN REAGENT,ACE TOTAL PROTEIN REAGENT,ACE BUN/UREANITROGEN REAGENT

K113253 Class I Traditional
Decision Date
2012-05-17
Sponsor / Applicant
Alfa Wassermann Diagnostic Technologies, Inc.

Technical Specification

510(k) Submission ID K113253
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 2012-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE AXCEL CLINICAL CHEMISTRY SYSTEM,ACE ALBUMIN REAGENT,ACE TOTAL PROTEIN REAGENT,ACE BUN/UREANITROGEN REAGENT received FDA 510(k) clearance under submission number K113253, sponsored by Alfa Wassermann Diagnostic Technologies, Inc.. 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 2012-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.