meddevicedb.com FDA Device Reference

HCG SOLID PHASE COMPONENT SYSTEM

K864591 Class II Traditional
Decision Date
1987-02-04
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K864591
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1987-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HCG SOLID PHASE COMPONENT SYSTEM received FDA 510(k) clearance under submission number K864591, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1987-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.