meddevicedb.com FDA Device Reference

QUALICODE B. BURGDORFERI IGM WESTERN BLOT KIT, MODEL DK-C062-024

K991062 Class II Traditional
Decision Date
1999-09-21
Sponsor / Applicant
Immunetics, Inc.

Technical Specification

510(k) Submission ID K991062
Product Code LSR
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3830
Decision Date 1999-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUALICODE B. BURGDORFERI IGM WESTERN BLOT KIT, MODEL DK-C062-024 received FDA 510(k) clearance under submission number K991062, sponsored by Immunetics, 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 1999-09-21.

Classification & Regulation

This clearance is catalogued under FDA product code LSR and 21 CFR 866.3830, within the Microbiology review panel as a Class II device.