K241411
- 510(k) number
- K241411
- Device name
- Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)
- Applicant
- Welch Allyn, Inc. NY · US
- Product code
- MWI — Monitor, Physiological, Patient (Without Arrhythmia
- Decision date
- 2024-12-20
- Date received
- 2024-05-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K241411.pdf
Official FDA record: K241411
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.