510(k) K032443 ยท IZI System, X-Ray, Angiographic
DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE
| Applicant | Shimadzu Corp., Torrance CA, US |
| Decision | Substantially Equivalent, Feb 20, 2004 |
| Received | Aug 8, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K032443
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.