510(k) K161767 ยท DXJ Display, Cathode-Ray Tube, Medical
Philips IntelliVue GuardianSoftware
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Jan 27, 2017 |
| Received | Jun 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161767
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.