510(k) K040675 ยท OWB Interventional Fluoroscopic X-Ray System
AXIOM ARTIS U
| Applicant | Siemens Medical Systems, Inc., Mavern PA, US |
| Decision | Substantially Equivalent, Jun 10, 2004 |
| Received | Mar 12, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040675
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 11, 2011 | Siemens Medical Solutions USA, Inc Siemens Axiom Artis U mobile x-ray system
Product Usage: Mobile x-ray system Terminated |
IZL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.