510(k) K980600 ยท JOW Sleeve, Limb, Compressible
D903 AVANT ADULT HOLLOW FIBER OXYGENATOR
| Applicant | Dideco S.P.A., North Attleboro MA, US |
| Decision | Substantially Equivalent, Aug 12, 1998 |
| Received | Feb 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980600
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.