meddevicedb.com FDA Device Reference

DUPONT ACA(R) PLUS IMMUNOASSAY SYS FERRITIN(FERR) METH

K935528 Class II Traditional
Decision Date
1994-01-28
Sponsor / Applicant
E.I. Dupont DE Nemours & Co., Inc.

Technical Specification

510(k) Submission ID K935528
Product Code DBF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5340
Decision Date 1994-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUPONT ACA(R) PLUS IMMUNOASSAY SYS FERRITIN(FERR) METH received FDA 510(k) clearance under submission number K935528, sponsored by E.I. Dupont DE Nemours & Co., 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 1994-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code DBF and 21 CFR 866.5340, within the Immunology review panel as a Class II device.