510(k) K820201 ยท DRS Transducer, Blood-Pressure, Extravascular
DISPOS. MONITORING SYS/LI ET AL
| Applicant | Linton Biomed Corp., Walker MI, US |
| Decision | Substantially Equivalent, Feb 12, 1982 |
| Received | Jan 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820201
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.