meddevicedb.com FDA Device Reference

Piccolo Potassium Test System

K200865 Class II Dual Track
Decision Date
2021-10-20
Sponsor / Applicant
Abaxis, Inc.

Technical Specification

510(k) Submission ID K200865
Product Code MZV
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 2021-10-20
Clearance Pathway Dual Track

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Piccolo Potassium Test System received FDA 510(k) clearance under submission number K200865, sponsored by Abaxis, Inc.. The device was reviewed via the Dual Track premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2021-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code MZV and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.