meddevicedb.com FDA Device Reference

GILFORD C4 COMPLEMENT REAGENT

K853468 Class II Traditional
Decision Date
1985-09-16
Sponsor / Applicant
Gilford

Technical Specification

510(k) Submission ID K853468
Product Code DBI
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5240
Decision Date 1985-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GILFORD C4 COMPLEMENT REAGENT received FDA 510(k) clearance under submission number K853468, sponsored by Gilford. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1985-09-16.

Classification & Regulation

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