LIFEPAK® ECG Cables
FDA 510(k) K240377 · Stryker Physio-Control
510(k) numberK240377
Submission
- Device name
- LIFEPAK® ECG Cables
- Applicant
- Stryker Physio-Control
Redmond, WA, US - Received
- February 7, 2024
- Decision date
- May 7, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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
Other 510(k)s with product code DSA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254114 | Baylis Connector CableDSA · Special | Baylis Medical Technologies, Inc. | 01/18/2026SE |
| K252827 | IBP cable Becton Dickinson (2606488); IBP cable Edwards (2606489); IBP cable Abbott…DSA · Traditional | Drägerwerk AG & Co. KGaA | 12/01/2025SE |
| K251669 | IBP transducer adapter cable, Argon/BD/Ohmeda, 2m; IBP transducer adapter cable, Draeger…DSA · Traditional | Shanghai Draeger Medical Instrument Co., Ltd. | 09/30/2025SE |
| K242986 | SpO2 Extension CableDSA · Special | Beijing Rongrui-Century Science & Technology… | 05/02/2025SE |
| K243545 | Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171…DSA · Traditional | Philips Medizin Systeme Böblingen GmbH | 01/17/2025SE |
| K240087 | RT Carbon ECG LeadsDSA · Traditional | Ivy Biomedical Systems, Inc. | 09/13/2024SE |
| K240156 | LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV…DSA · Traditional | Physio-Control, Inc. | 04/30/2024SE |
| K222712 | Fogg System Patient Monitoring CablesDSA · Traditional | Fogg System Company, Inc. | 11/22/2023SE |
| K230571 | RFP-100A Connector Cable (Single Use)DSA · Traditional | Baylis Medical Technologies, Inc. | 05/30/2023SE |
| K222370 | SpO2 Extension CableDSA · Traditional | Beijing Rongrui-Century Science & Technology… | 04/02/2023SE |
More from Beijing Rongrui-Century Science & Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K240162 | LIFEPAK® 35 AC Power Adapter (41335-000001)MPD · Traditional | 04/19/2024SE |
Questions and answers
When was LIFEPAK® ECG Cables cleared by the FDA?
LIFEPAK® ECG Cables (K240377) received a 510(k) decision of Substantially Equivalent on May 7, 2024, 90 days after the submission was received.
What is the product code of K240377?
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.