510(k) K180534 ยท DXJ Display, Cathode-Ray Tube, Medical
Philips IntelliVue GuardianSoftware
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Jul 16, 2018 |
| Received | Feb 28, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180534
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.