510(k) K913595 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
| Applicant | Koven and Assoc., Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 27, 1992 |
| Received | Aug 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913595
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.