510(k) K833672 ยท LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular
HH SUBCUTANEOUS ACCESS PORT
| Applicant | Holter-Hausner Intl., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 6, 1984 |
| Received | Oct 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833672
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.