510(k) K820102 ยท DQR Cannula, Catheter
SUBCLAVIAN JUGULAR CATHETER SET
| Applicant | Luther Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 29, 1982 |
| Received | Jan 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820102
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.