Neteera 130H-Plus Vital Sign Monitoring Sensor— 510(k) K231733
Substantially EquivalentNeteera Technologies , Ltd.
FDA 510(k) clearance K231733 for Neteera 130H-Plus Vital Sign Monitoring Sensor, Substantially Equivalent on 2024-02-09. Applicant: Neteera Technologies , Ltd..
Clearance details
- Applicant
- Neteera Technologies , Ltd.
- Product code
- Code DRT
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jerusalem, IL
Adverse events under product code DRT
product code DRT- Death
- 4
- Total
- 4
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.