510(k) K833822 ยท LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular
P-S MEDICAL CSF ACCESS DEV 15MM/25MM
| Applicant | Pudenz-Schulte Medical Research Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 25, 1984 |
| Received | Nov 2, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833822
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.