510(k) K842486 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ELECTRONIC DIGITAL BP METER HC 3001
| Applicant | North American Philips Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 24, 1984 |
| Received | Jun 26, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842486
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.