510(k) K212003 ยท DXJ Display, Cathode-Ray Tube, Medical
ESSENZ Patient Monitor
| Applicant | Livanova Deutschland, GmbH, Munich, DE |
| Decision | Substantially Equivalent, Nov 10, 2021 |
| Received | Jun 28, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212003
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.