510(k) K903193 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
SMITH & NEPHEW DYONICS LEVELERT SYSTEM
| Applicant | Smith & Nephew Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Aug 30, 1990 |
| Received | Jul 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903193
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.