meddevicedb.com FDA Device Reference

IFA TEST FOR ANTIBODIES TO BORRELIA BURGDORFERI

K871246 Class II Traditional
Decision Date
1987-08-25
Sponsor / Applicant
Zeus Scientific, Inc.

Technical Specification

510(k) Submission ID K871246
Product Code LSR
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3830
Decision Date 1987-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IFA TEST FOR ANTIBODIES TO BORRELIA BURGDORFERI received FDA 510(k) clearance under submission number K871246, sponsored by Zeus Scientific, 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 1987-08-25.

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.