510(k) K820202 ยท DRS Transducer, Blood-Pressure, Extravascular
CONTINUOUS FLUSH DEVICE/FDI
| Applicant | Linton Biomed Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 12, 1982 |
| Received | Jan 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820202
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.