meddevicedb.com FDA Device Reference

ACE ALBUMIN REAGENT, ACE TOTAL PROTEIN REAGENT, ACE CALCIUM-ARSENAZO REAGENT AND ACE PHOSPHORUS REAGENT

K131488 Class II Traditional
Decision Date
2013-08-19
Sponsor / Applicant
Alfa Wassermann Diagnostics Technologies, LLC

Technical Specification

510(k) Submission ID K131488
Product Code CIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1035
Decision Date 2013-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE ALBUMIN REAGENT, ACE TOTAL PROTEIN REAGENT, ACE CALCIUM-ARSENAZO REAGENT AND ACE PHOSPHORUS REAGENT received FDA 510(k) clearance under submission number K131488, sponsored by Alfa Wassermann Diagnostics Technologies, 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 2013-08-19.

Classification & Regulation

This clearance is catalogued under FDA product code CIX and 21 CFR 862.1035, within the Clinical Chemistry review panel as a Class II device.