510(k) K900682 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
PHANTOM RADIOTRANSLUCENT ECG MONITORING ELECTRODE
| Applicant | Contour Electrodes, Inc., Herrin IL, US |
| Decision | Substantially Equivalent, Jul 31, 1990 |
| Received | Feb 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900682
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.