510(k) K901228 ยท FKX System, Peritoneal, Automatic Delivery
MULTI-STRIP
| Applicant | Bellhouse Medical, Inc., Lake Elmo MN, US |
| Decision | Substantially Equivalent, May 7, 1990 |
| Received | Mar 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901228
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.