510(k) K151736 ยท DXJ Display, Cathode-Ray Tube, Medical
Philips IntelliVue GuardianSoftware
| Applicant | Philips Medizin Systeme Boblingen GmbH, Boblingen, DE |
| Decision | Substantially Equivalent, Oct 21, 2015 |
| Received | Jun 26, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151736
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.