510(k) K060123 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
LEVELERT II FLUID LEVEL SENSOR
| Applicant | Smith & Nephew, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Feb 14, 2006 |
| Received | Jan 18, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060123
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.