510(k) K830686 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
ANEROID BLOOD PRESSURE CUFF #HC1400
| Applicant | North American Philips Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 18, 1983 |
| Received | Mar 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830686
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.