510(k) K800703 ยท DQO Catheter, Intravascular, Diagnostic
MODIFIED CATHETER PACKAGE
| Applicant | Hancock Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 8, 1980 |
| Received | Mar 27, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800703
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.