510(k) K810840 ยท KDJ Set, Administration, For Peritoneal Dialysis, Disposable
AMP PERITONEAL DIALYSIS PREP KIT
| Applicant | American Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 29, 1981 |
| Received | Mar 27, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810840
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.