510(k) K915337 ยท DTW Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
CAPIOX LEVEL ALARM
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Feb 21, 1992 |
| Received | Nov 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915337
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.