510(k) K103802 ยท DQA Oximeter
TRUSIGNAL R SPO2 PEDITIP SENSOR; TRUSIGNAL R SPO2 PEDITIP SENSOR; TRUSIGNAL R SPO2 PEDITIP SENSOR
| Applicant | GE Healthcare Finland Oy, Helsinki, FI |
| Decision | Substantially Equivalent, Aug 2, 2011 |
| Received | Dec 28, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103802
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.