510(k) K770290 ยท DQO Catheter, Intravascular, Diagnostic
MONITORING KIT, CENTRAL VENOUS PRESSURE
| Applicant | Argon Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 15, 1977 |
| Received | Feb 14, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770290
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.