510(k) K896633 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
AUTO-CUFF(TM)
| Applicant | U.S. Medical Corp., Cheshire CT, US |
| Decision | Substantially Equivalent, Feb 1, 1990 |
| Received | Nov 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896633
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.