510(k) K153232 ยท OWB Interventional Fluoroscopic X-Ray System
Cios Select
| Applicant | Siemens Medical Solutions USA, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Feb 10, 2016 |
| Received | Nov 9, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K153232
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.