510(k) K092153 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
SKYLINE 55, MODEL VER 1
| Applicant | Larsen & Toubro Limited, Schaumburg IL, US |
| Decision | Substantially Equivalent, Nov 20, 2009 |
| Received | Jul 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092153
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.