510(k) K921343 ยท DRS Transducer, Blood-Pressure, Extravascular
COBE PATIENT MONITORING PRODUCTS
| Applicant | Cobe Cardiovascular, Inc., Arvada CO, US |
| Decision | Substantially Equivalent, Jan 5, 1993 |
| Received | Mar 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921343
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.