510(k) K212208 ยท DXJ Display, Cathode-Ray Tube, Medical
Philips IntelliVue GuardianSoftware (Rev. E.0X)
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Sep 30, 2021 |
| Received | Jul 15, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212208
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.