510(k) K881006 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
STOCKERT-SHILEY BUBBLE MONITOR 23-23-01
| Applicant | Shiley, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 24, 1988 |
| Received | Mar 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881006
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.