510(k) K884912 ยท IZI System, X-Ray, Angiographic
ANGIOSTAR
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Feb 16, 1989 |
| Received | Nov 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884912
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 10, 2009 | Siemens Medical Solutions USA, Inc Koodinat M/MP Patient Table used with Angiostar Model 5294009.
The device is used as an Angiographic X-Ray System. Terminated |
IZI | None listed |
| Nov 4, 2008 | Siemens Medical Solutions USA, Inc ANGIOSTAR X-Ray System, Model numbers 9359142 and 6379668. Terminated |
IZI | None listed |
| Nov 4, 2008 | Siemens Medical Solutions USA, Inc ANGIOSTAR Plus X-Ray System, Model number 6379718. Terminated |
IZI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.