510(k) K170514 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Central Monitoring System
| Applicant | Guangdong Biolight Meditech Co., Ltd., Zhuhai, CN |
| Decision | Substantially Equivalent, May 24, 2017 |
| Received | Feb 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170514
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.