510(k) K934385 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
MINIPACK 3100/3000 MODIFICATION
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Aug 10, 1994 |
| Received | Sep 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934385
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.