meddevicedb.com FDA Device Reference

LIAISON ANTI-HAV ASSAY, LIAISON CONTROL ANTI-HAV

K082049 Class II Traditional
Decision Date
2008-12-05
Sponsor / Applicant
DiaSorin, Inc.

Technical Specification

510(k) Submission ID K082049
Product Code LOL
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3310
Decision Date 2008-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIAISON ANTI-HAV ASSAY, LIAISON CONTROL ANTI-HAV received FDA 510(k) clearance under submission number K082049, sponsored by DiaSorin, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2008-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code LOL and 21 CFR 866.3310, within the Microbiology review panel as a Class II device.