510(k) K173941 ยท HGM System, Monitoring, Perinatal
IntelliSpace Perinatal Rev.K.00
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Sep 10, 2018 |
| Received | Dec 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173941
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.