K240377
- 510(k) number
- K240377
- Device name
- LIFEPAK® ECG Cables
- Applicant
- Stryker Physio-Control WA · US
- Product code
- DSA — Cable, Transducer And Electrode, Patient, (Including
- Decision date
- 2024-05-07
- Date received
- 2024-02-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K240377.pdf
Official FDA record: K240377
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.