510(k) K030136 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
DRIP ALERT
| Applicant | Drip Alert, Inc., Ft. Lauderdale FL, US |
| Decision | Substantially Equivalent, Apr 7, 2003 |
| Received | Jan 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030136
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.