510(k) K173507 ยท LNH System, Nuclear Magnetic Resonance Imaging
Prodiva 1.5T CX and Prodiva 1.5T CS R5.4
| Applicant | Philips Healthcare (Suzhou) Co., Ltd., Suzhou, CN |
| Decision | Substantially Equivalent, Jun 15, 2018 |
| Received | Nov 13, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K173507
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.