510(k) K973472 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
3M CDI H/S CUVETTES WITH HEPARON TREATMENT
| Applicant | 3M Healthcare, Tistin CA, US |
| Decision | Substantially Equivalent, Dec 8, 1997 |
| Received | Sep 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973472
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.