510(k) K173187 ยท IZL System, X-Ray, Mobile
MobileDiagnost M50
| Applicant | Philips India Limited, Pune, IN |
| Decision | Substantially Equivalent, Nov 16, 2017 |
| Received | Oct 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173187
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.