510(k) K914164 ยท BXN Stimulator, Nerve, Battery-Powered
VITALMAX 840 SERIES
| Applicant | Pace Tech Medical Monitors, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Apr 9, 1993 |
| Received | Sep 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914164
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.