510(k) K802602 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
L-3 PURGE LINE
| Applicant | Delta Medical Industries, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Oct 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802602
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.