510(k) K900459 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
APPLICARD (EKG)
| Applicant | Medi-Globe Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Jul 31, 1990 |
| Received | Jan 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900459
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.