510(k) K823790 ยท LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular
VENTRICULAR ACCESS SYSTEM
| Applicant | American Heyer Schulte, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 28, 1983 |
| Received | Dec 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823790
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.