510(k) K161035 ยท DXQ Blood Pressure Cuff
Medline Singe Patient Use Blood Pressure Cuff
| Applicant | Medline Industries, Inc., Mundelein IL, US |
| Decision | Substantially Equivalent, Jun 13, 2016 |
| Received | Apr 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161035
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.