Dri-Vent Arterial Blood Sampling Kit

FDA 510(k) K883840 · Concord Laboratories, Inc.

Unknown

510(k) numberK883840

Submission

Device name
Dri-Vent Arterial Blood Sampling Kit
Applicant
Concord Laboratories, Inc.
Keene, NH, US
Received
September 12, 1988
Decision date
May 16, 1989
Decision
Unknown (SESD)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LKB – Pad, Alcohol, Device Disinfectant
Device class
Unclassified

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K112791Sitescrub Ipa DeviceLKB · Traditional C. R. Bard02/24/2012SE
K912161I.V. Starr KitLKB · Traditional Medical Device Inspection Co., Inc.10/08/1991SE
K912731Steri-SwabLKB · Traditional Westlock Investments (Usa), Inc.10/02/1991SE
K910735Hexidis Alcohol SwabLKB · Traditional Specialites Septodont04/02/1991SE
K896898Bowen Electrode Skin Prepatory CleanserLKB · Traditional Bowen & Company, Inc.04/04/1990SE
K896835Alcohol Prep and Povidone-Iodine PrepLKB · Traditional Norpak Mfg., Inc.01/11/1990SE
K894791Baxter Acetone-Alcohol Swabstick, SterileLKB · Traditional Span-America Medical Systems, Inc.10/03/1989SE
K893958Baxter Acetone-Alcohol Prep Pads, SterileLKB · Traditional Span-America Medical Systems, Inc.10/03/1989SE

More from Span-America Medical Systems, Inc.

510(k)DeviceDecision
K871825Meconium Suction CatheterBSY · Traditional 06/29/1987SE
K864535Tracheobronchial Suction Catheter, Cat. No. 6110BSY · Traditional 01/06/1987SE
K862039Concord Care Tray · Traditional 07/03/1986SESD
K854601Spring Guide Catheter Anesthesia Conduction CathBSO · Traditional 01/10/1986SE
K854327Subcutaneous Tunneling Needles & HandlesGCB · Traditional 11/13/1985SE
K851134Regional Anesthesia TraysCAZ · Traditional 07/15/1985SESD
K842095Epidural TraysCAZ · Traditional 07/03/1984SE
K841486Arterial Blood Sampling KitsCBT · Traditional 05/23/1984SE
K840987Vaporized HeparinCBT · Traditional 04/05/1984SE
K840986Prefilled Pulsator SyringeCBT · Traditional 04/05/1984SE

Questions and answers

When was Dri-Vent Arterial Blood Sampling Kit cleared by the FDA?

Dri-Vent Arterial Blood Sampling Kit (K883840) received a 510(k) decision of Unknown on May 16, 1989, 246 days after the submission was received.

What is the product code of K883840?

The FDA product code is LKB – Pad, Alcohol, Device Disinfectant, a Unclassified device.