510(k) K992603 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
XRT 600 R/F, WRF 0600
| Applicant | Wuestec Medical, Inc., Mobile AL, US |
| Decision | Substantially Equivalent, Oct 25, 1999 |
| Received | Aug 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992603
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.