Vacutainer Brand Blood Collection Syringe

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K982922 ↗

FDA Product Code

JKA

Device Class

Class II

Regulation

21 CFR Part 862.1675

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Vacutainer Brand Ppt Plasma Preparation Tube

  Class II

  FDA 510(k) K972075 Active Cleared 24 Feb 1998

• Microtainer Brand Chemistry Tubes with Microgard Closure, Model 365965, 365985, 365963, 365967, 36578

  Class II

  FDA 510(k) K991702 Active Cleared 28 Jul 1999

• Vacutainer Brand Eclipse Blood Collection Needle, Models# 368607 & 368608

  Class II

  FDA 510(k) K982541 Active Cleared 28 Oct 1998

• Vacutainer Plus Tubes

  Class II

  FDA 510(k) K953463 Active Cleared 20 Sep 1995

• Seditainer Erythrocyte Sedimentation Rate (ESR) System

  Class II

  FDA 510(k) K953994 Active Cleared 26 Sep 1995

• Lok-On Needle Disposal System

  Class II

  FDA 510(k) K951886 Active Cleared 30 Jun 1995

See all devices from Becton Dickinson Vacutainer Systems →