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VACUTAINER BRAND PLUS SERUM & SST TUBES

K960250 Class II Traditional
Decision Date
1996-03-29
Sponsor / Applicant
Becton Dickinson Vacutainer Systems

Technical Specification

510(k) Submission ID K960250
Product Code JKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1996-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VACUTAINER BRAND PLUS SERUM & SST TUBES received FDA 510(k) clearance under submission number K960250, sponsored by Becton Dickinson Vacutainer Systems. 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 1996-03-29.

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.