510(k) K971865 ยท LDR Controller, Infusion, Intravascular, Electronic
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P
| Applicant | Alexander Mfg. Co., Mason City IA, US |
| Decision | Substantially Equivalent, Jul 3, 1997 |
| Received | May 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971865
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.