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HCG SOLID PHASE COMPONENT SYSTEM

K901045 Class II Traditional
Decision Date
1990-03-29
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K901045
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1990-03-29
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 K901045, 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 1990-03-29.

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.