510(k) K253196 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)
| Applicant | Midmark Corporation, Versailles OH, US |
| Decision | Substantially Equivalent, Jun 12, 2026 |
| Received | Sep 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253196
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.