510(k) K002962 ยท DQX Wire, Guide, Catheter
PRESSURE WIRE SENSOR, MODEL 12003/12303
| Applicant | Radi Medical Systems AB, Uppsala, SE |
| Decision | Substantially Equivalent, Oct 4, 2000 |
| Received | Sep 22, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K002962
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.