510(k) K924354 ยท DTW Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITOR
| Applicant | Sorin Biomedica, Fiat, USA, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 18, 1993 |
| Received | Aug 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924354
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.