meddevicedb.com FDA Device Reference

NYCOCARD CRP

K013787 Class II Traditional
Decision Date
2002-05-14
Sponsor / Applicant
Primus Corp.

Technical Specification

510(k) Submission ID K013787
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2002-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NYCOCARD CRP received FDA 510(k) clearance under submission number K013787, sponsored by Primus Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2002-05-14.

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.