510(k) K982319 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
CAREGRAPH
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Sep 22, 1998 |
| Received | Jul 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982319
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.