Dri-Vent Arterial Blood Sampling Kit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K883840 ↗

FDA Product Code

LKB

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESD Substantially Equivalent — Deferred

• Prefilled Pulsator Syringe

  Class II

  FDA 510(k) K811009 Active Cleared 12 Jun 1981

• Epidural Trays

  Class II

  FDA 510(k) K842095 Active Cleared 3 Jul 1984

• Syringe, Blood Sampling, Arterial, #4015

  Class II

  FDA 510(k) K770852 Active Cleared 14 Jul 1977

• Arterial Blood Sampling Kits

  Class I

  FDA 510(k) K841486 Active Cleared 23 May 1984

• Tray, Blood Sampling (Pulsator II)

  Class II

  FDA 510(k) K760086 Active Cleared 16 Jul 1976

• Sani Catch Ba

  Class I

  FDA 510(k) K833814 Active Cleared 19 Mar 1984

See all devices from Concord Laboratories, Inc. →