510(k) K131762 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
HANDHELD MONITOR
| Applicant | Guangdong Biolight Meditech Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Jun 6, 2014 |
| Received | Jun 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131762
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.