meddevicedb.com FDA Device Reference

VACUTAINER BRAND SAFETY-LOK BLOOD COLLECTION SET

K965202 Class II Traditional
Decision Date
1997-02-10
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K965202
Product Code JKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1997-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VACUTAINER BRAND SAFETY-LOK BLOOD COLLECTION SET received FDA 510(k) clearance under submission number K965202, 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 1997-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.