510(k) K792088 ยท DWS Instruments, Surgical, Cardiovascular
AORTIC OCCLUDER #000390
| Applicant | Edward Weck, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 26, 1979 |
| Received | Oct 17, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792088
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.