K231733
- 510(k) number
- K231733
- Device name
- Neteera 130H-Plus Vital Sign Monitoring Sensor
- Applicant
- Neteera Technologies , Ltd. IL
- Product code
- DRT — Monitor, Cardiac (Incl. Cardiotachometer & Rate Alar
- Decision date
- 2024-02-09
- Date received
- 2023-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231733.pdf
Official FDA record: K231733
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.