510(k) K820222 ยท DYG Catheter, Flow Directed
SWAN-GANZ VIP-CATHETER
| Applicant | American Edwards Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 12, 1982 |
| Received | Jan 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820222
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.