510(k) K001388 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
DATA MASTER PERFUSION MONITORING SYSTEM
| Applicant | Dideco, North Attleboro MA, US |
| Decision | Substantially Equivalent, Jul 28, 2000 |
| Received | May 2, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K001388
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.