510(k) K822548 ยท FKX System, Peritoneal, Automatic Delivery
SAFE LOCK CATHETER S-3
| Applicant | American Medical Products, Inc., Freehold NJ, US |
| Decision | Substantially Equivalent, Oct 13, 1982 |
| Received | Aug 24, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822548
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.