510(k) K181919 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Patient Monitor
| Applicant | Guangdong Biolight Meditech Co., Ltd., Zhuhai, CN |
| Decision | Substantially Equivalent, Apr 5, 2019 |
| Received | Jul 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181919
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.