510(k) K953835 ยท DTZ Oxygenator, Cardiopulmonary Bypass
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
| Applicant | Dideco S.R.L., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 15, 1996 |
| Received | Aug 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953835
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.