510(k) K060749 ยท IZI System, X-Ray, Angiographic
XPERCT
| Applicant | Philips Medical Systems North America Co., Bothell WA, US |
| Decision | Substantially Equivalent, Apr 4, 2006 |
| Received | Mar 20, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060749
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.