Secure Arterial Blood Sampling System

FDA 510(k) K070340 · Smiths Medical Asd, Inc.

Substantially Equivalent

510(k) numberK070340

Submission

Device name
Secure Arterial Blood Sampling System
Applicant
Smiths Medical Asd, Inc.
Dublin, OH, US
Received
February 6, 2007
Decision date
March 15, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CBT – Arterial Blood Sampling Kit
Device class
Class I (low risk)
Regulation
21 CFR 868.1100
Specialty
Anesthesiology

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Other 510(k)s with product code CBT

510(k)DeviceApplicantDecision
K071269Hemodraw Arterial Blood Sampling SystemCBT · Traditional Smiths Medical Asd, Inc.08/01/2007SE
K955663Abc In-Line Blood Sampling KitCBT · Traditional Utah Medical Products, Inc.03/17/1997SE
K954015Abg Point Lok Needle Protection DeviceCBT · Traditional Devon Industries, Inc.11/20/1995SE
K954035Acti-Flex Arterial Extension SetCBT · Traditional R-Group Intl.09/25/1995SE
K950098Needle Safety CoverCBT · Traditional Hammer-Plane, Inc.08/11/1995SE
K945719Aspir-Pulse(Tm) Arterial Blood Gas (Abg) SystemCBT · Traditional Sherwood Medical Co.03/16/1995SESK
K944941Piston SyringeCBT · Traditional Martell Medical Products, Inc.12/05/1994SE
K945485Abg Needle ProtectionCBT · Traditional Devon Industries, Inc.11/29/1994SE
K940575Aspir-Pulse(Tm) Saf-T-VentCBT · Traditional Sherwood Medical Co.03/22/1994SE
K931873VacventCBT · Traditional Steven Frank Mercereau12/30/1993SEKD

More from Steven Frank Mercereau

510(k)DeviceDecision
K232943Hypodermic Needle-Pro® EDGE™ Safety Device with Low Dead Space SyringeQNQ · Traditional 05/31/2024SE
K210833Portex BLUxl Extra Length Tracheostomy Tube, BLUxl Suctionaid Extra Length Tracheostomy…JOH · Traditional 11/26/2021SE
K211634Hypodermic Needle-Pro EDGE Safety DeviceFMI · Special 08/26/2021SE
K192375Intellifuse Administration and Intellifuse Blood Administration SetsFPA · Traditional 09/18/2020SE
K181699Level 1 Convective WarmerDWJ · Traditional 07/26/2018SE
K172800Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal…MIA · Traditional 06/14/2018SE
K172823Portex NRFit Epidural NeedlesBSP · Traditional 06/12/2018SE
K172410Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of…BSP · Traditional 06/01/2018SE
K172592CADD Yellow High Volume Administration Set with NRFit connectorPWH · Traditional 05/17/2018SE
K173912BLUperc Percutaneous Dilation Tracheostomy Kit with BLUselect tube, BLUperc Percutaneous…JOH · Traditional 05/08/2018SE

Questions and answers

When was Secure Arterial Blood Sampling System cleared by the FDA?

Secure Arterial Blood Sampling System (K070340) received a 510(k) decision of Substantially Equivalent on March 15, 2007, 37 days after the submission was received.

What is the product code of K070340?

The FDA product code is CBT – Arterial Blood Sampling Kit, a Class I (low risk) device regulated under 21 CFR 868.1100.