meddevicedb.com FDA Device Reference

KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT

K051061 Class II Traditional
Decision Date
2005-11-04
Sponsor / Applicant
Kronus Market Development Associates, Inc.

Technical Specification

510(k) Submission ID K051061
Product Code NWG
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5660
Decision Date 2005-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT received FDA 510(k) clearance under submission number K051061, sponsored by Kronus Market Development Associates, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2005-11-04.

Classification & Regulation

This clearance is catalogued under FDA product code NWG and 21 CFR 866.5660, within the Immunology review panel as a Class II device.