510(k) K851888 ยท DRS Transducer, Blood-Pressure, Extravascular
APM DISPOS. BLOOD PRESSURE TRANSDUCER
| Applicant | Honeywell, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Aug 6, 1985 |
| Received | May 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851888
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.