LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024)

FDA 510(k) K240156 · Physio-Control, Inc.

Substantially Equivalent

510(k) numberK240156

Submission

Device name
LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024)
Applicant
Physio-Control, Inc.
Redmond, WA, US
Received
January 19, 2024
Decision date
April 30, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DSA – Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2900
Specialty
Cardiovascular

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K254114Baylis Connector CableDSA · Special Baylis Medical Technologies, Inc.01/18/2026SE
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K251669IBP transducer adapter cable, Argon/BD/Ohmeda, 2m; IBP transducer adapter cable, Draeger…DSA · Traditional Shanghai Draeger Medical Instrument Co., Ltd.09/30/2025SE
K242986SpO2 Extension CableDSA · Special Beijing Rongrui-Century Science & Technology…05/02/2025SE
K243545Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171…DSA · Traditional Philips Medizin Systeme Böblingen GmbH01/17/2025SE
K240087RT Carbon ECG LeadsDSA · Traditional Ivy Biomedical Systems, Inc.09/13/2024SE
K240377LIFEPAK® ECG CablesDSA · Traditional Stryker Physio-Control05/07/2024SE
K222712Fogg System Patient Monitoring CablesDSA · Traditional Fogg System Company, Inc.11/22/2023SE
K230571RFP-100A Connector Cable (Single Use)DSA · Traditional Baylis Medical Technologies, Inc.05/30/2023SE
K222370SpO2 Extension CableDSA · Traditional Beijing Rongrui-Century Science & Technology…04/02/2023SE

More from Beijing Rongrui-Century Science & Technology Co., Ltd.

510(k)DeviceDecision
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K182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsLDD · Traditional 06/03/2019SE
K142430LIFEPAK 15 monitor/defibrillatorMKJ · Traditional 12/19/2014SE
K130454Lifepak 20 Defibrillator/Monitor, Lifepak 20E Defibrillator/MonitorMKJ · Traditional 08/21/2013SE
K123597Truecpr Coaching DeviceLIX · Traditional 04/17/2013SE
K122600Lifepak 1000 DefibrillatorMKJ · Traditional 10/11/2012SE
K103567Lifepak 15 Monitor/DefibrillatorMKJ · Traditional 03/22/2011SE
K102972Lifepak 12MKJ · Special 12/22/2010SE
K102757Lifenet SystemMSX · Special 11/05/2010SE
K093925Lifenet SystemMSX · Special 01/12/2010SE

Questions and answers

When was LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024) cleared by the FDA?

LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024) (K240156) received a 510(k) decision of Substantially Equivalent on April 30, 2024, 102 days after the submission was received.

What is the product code of K240156?

The FDA product code is DSA – Cable, Transducer And Electrode, Patient, (Including Connector), a Class II (moderate risk) device regulated under 21 CFR 870.2900.