K242018
- 510(k) number
- K242018
- Device name
- UbiqVue 2A Multi-parameter System (UX2550)
- Applicant
- Lifesignals, Inc. CA · US
- Product code
- DRG — Transmitters And Receivers, Physiological Signal, Ra
- Decision date
- 2024-11-12
- Date received
- 2024-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K242018.pdf
Official FDA record: K242018
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.