510(k) K915255 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
CDI(TM) 300, 400 & 100, MODIFICATION
| Applicant | 3M Company, Tustin CA, US |
| Decision | Substantially Equivalent, Jan 15, 1992 |
| Received | Nov 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915255
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.