510(k) K843273 ยท DRS Transducer, Blood-Pressure, Extravascular
DISPOS. PRESSURE KIT 1295K SERIES
| Applicant | Hewlett-Packard Co., Walker MI, US |
| Decision | Substantially Equivalent, Jun 11, 1985 |
| Received | Aug 20, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843273
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.