510(k) K231733 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Neteera 130H-Plus Vital Sign Monitoring Sensor
| Applicant | Neteera Technologies , Ltd., Jerusalem, IL |
| Decision | Substantially Equivalent, Feb 9, 2024 |
| Received | Jun 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231733
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.