510(k) K082685 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
GALAXY 55
| Applicant | Larsen & Toubro Limited, Schaumburg IL, US |
| Decision | Substantially Equivalent, Sep 26, 2008 |
| Received | Sep 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082685
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.