510(k) K902401 ยท FMF Syringe, Piston
CELSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM
| Applicant | Burron Medical, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Oct 8, 1991 |
| Received | May 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902401
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.