510(k) K021239 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-400M
| Applicant | Eikon Healthcare Device Corp., Hsin-Chu City,, TW |
| Decision | Substantially Equivalent, Nov 8, 2002 |
| Received | Apr 18, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021239
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.