510(k) K935461 ยท FIH Pump, Infusion Or Syringe, Extra-Luminal
VECTOR AMBULATORY DRUG DELIVERY SYSTEM
| Applicant | Infusion Technology Intl., Danvers MA, US |
| Decision | Substantially Equivalent, Apr 28, 1994 |
| Received | Nov 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935461
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.