510(k) K093017 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
STELLAR 300
| Applicant | Larsen & Toubro Limited, Crofton MD, US |
| Decision | Substantially Equivalent, Apr 29, 2010 |
| Received | Sep 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093017
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.