meddevicedb.com FDA Device Reference

BIOSTAR RE-A-DS IMMUNE COMPLEX ASSAY KIT

K853697 Class II Traditional
Decision Date
1985-12-16
Sponsor / Applicant
Biostar Medical Products, Inc.

Technical Specification

510(k) Submission ID K853697
Product Code DAK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5240
Decision Date 1985-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSTAR RE-A-DS IMMUNE COMPLEX ASSAY KIT received FDA 510(k) clearance under submission number K853697, sponsored by Biostar Medical Products, 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 1985-12-16.

Classification & Regulation

This clearance is catalogued under FDA product code DAK and 21 CFR 866.5240, within the Immunology review panel as a Class II device.