510(k) K842352 ยท DRS Transducer, Blood-Pressure, Extravascular
PRESSURE MONITORING KIT
| Applicant | Utah Medical Products, Inc., Lehi UT, US |
| Decision | Substantially Equivalent, Mar 25, 1985 |
| Received | Jun 15, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842352
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.