510(k) K172242 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
DripAssist Plus
| Applicant | Shift Labs, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, May 25, 2018 |
| Received | Jul 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172242
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.