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DU PONT DIMENSION C-REACTIVE PROTEIN CALIBRATOR

K884101 Class II Traditional
Decision Date
1988-10-19
Sponsor / Applicant
E.I. Dupont DE Nemours & Co., Inc.

Technical Specification

510(k) Submission ID K884101
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 1988-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DU PONT DIMENSION C-REACTIVE PROTEIN CALIBRATOR received FDA 510(k) clearance under submission number K884101, 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 1988-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code DCK and 21 CFR 866.5270, within the Immunology review panel as a Class II device.