K233133
- 510(k) number
- K233133
- Device name
- Talis EMR with Talis +ACG (Talis EMR with +ACG)
- Applicant
- Talis Clinical, LLC OH · US
- Product code
- MWI — Monitor, Physiological, Patient (Without Arrhythmia
- Decision date
- 2024-04-01
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K233133.pdf
Official FDA record: K233133
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.