meddevicedb.com FDA Device Reference

HUMAN ALPHA-1 ANTITRYPSIN KIT SPAPLUS

K123256 Class II Traditional
Decision Date
2013-07-03
Sponsor / Applicant
The Binding Site Group , Ltd.

Technical Specification

510(k) Submission ID K123256
Product Code DEM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5130
Decision Date 2013-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUMAN ALPHA-1 ANTITRYPSIN KIT SPAPLUS received FDA 510(k) clearance under submission number K123256, sponsored by The Binding Site Group , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2013-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code DEM and 21 CFR 866.5130, within the Immunology review panel as a Class II device.