510(k) K020739 ยท DQA Oximeter
BCI 3178 PEDIATRIC PULSE OXIMETRY SENSOR
| Applicant | Bci, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Jun 3, 2002 |
| Received | Mar 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020739
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.