510(k) K983506 ยท DQX Wire, Guide, Catheter
PRESSUREWIRE SENSOR, MODEL #12001
| Applicant | Radi Medical Systems AB, Uppsala, SE |
| Decision | Substantially Equivalent, Feb 3, 1999 |
| Received | Oct 7, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983506
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.