510(k) K800122 ยท DWS Instruments, Surgical, Cardiovascular
HANCOCK AORTIC PUNCH
| Applicant | Hancock Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 1, 1980 |
| Received | Jan 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800122
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.