510(k) K933687 ยท FKX System, Peritoneal, Automatic Delivery
R & D BATTERIES,INC. PART NUMBERS 5164, 5272, 5260
| Applicant | R & D Batteries, Inc., Burnsville MN, US |
| Decision | Substantially Equivalent, Feb 9, 1994 |
| Received | Jul 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933687
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.