510(k) K143332 ยท DXQ Blood Pressure Cuff
Fast Sphyg by Koven
| Applicant | Koven Technology, Inc., St Louis MO, US |
| Decision | Substantially Equivalent, Apr 14, 2015 |
| Received | Nov 20, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143332
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.