510(k) K823764 ยท DWS Instruments, Surgical, Cardiovascular
SCANLAN SINGLE-USE AORTA PUNCH
| Applicant | Scanlan Intl., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 24, 1983 |
| Received | Dec 14, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823764
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.