510(k) K103763 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
STELLAR 300
| Applicant | Larsen & Toubro Limited, Crofton MD, US |
| Decision | Substantially Equivalent, Mar 11, 2011 |
| Received | Dec 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103763
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.