510(k) K913042 ยท DXO Transducer, Pressure, Catheter Tip
MODIFICATIONS TO SERIES OF CARDIAC CATHETERS
| Applicant | Sentron, Inc., Federal Way WA, US |
| Decision | Substantially Equivalent, Oct 21, 1992 |
| Received | Jun 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913042
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.