510(k) K862344 ยท DRS Transducer, Blood-Pressure, Extravascular
GOULD XCALIBER
| Applicant | Bio-Tek Instruments, Inc., Winooski VT, US |
| Decision | Substantially Equivalent, Aug 6, 1986 |
| Received | Jun 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862344
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.