510(k) K901733 ยท DPW Flowmeter, Blood, Cardiovascular
MODIFIED FLOCATH PULMONARY ARTERY CATHETER
| Applicant | Cardio Metrics, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 16, 1990 |
| Received | Apr 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901733
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.