510(k) K021154 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
GOLDWAY PATIENT MONITOR, MODEL # UT4000F
| Applicant | Goldway Us, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Apr 11, 2003 |
| Received | Apr 10, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021154
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.