510(k) K973598 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
SIREMOBIL CO2
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Nov 10, 1997 |
| Received | Sep 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973598
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 2, 2005 | Siemens Medical Solutions USA, Inc Powermobil 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.