510(k) K964990 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
HITACHI SX-VA30 C-ARM FLUOROSCOPIC/ANGIOGRAPHIC SYSTEM (SX-VA30)
| Applicant | Hitachi Medical Systems America, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, Feb 26, 1997 |
| Received | Dec 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964990
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.