meddevicedb.com FDA Device Reference

AFINION ANALYZER

K110056 Class II Traditional
Decision Date
2011-02-15
Sponsor / Applicant
Axis-Shield Poc AS

Technical Specification

510(k) Submission ID K110056
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 2011-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AFINION ANALYZER received FDA 510(k) clearance under submission number K110056, sponsored by Axis-Shield Poc AS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2011-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.