510(k) K020365 ยท KRI Accessory Equipment, Cardiopulmonary Bypass
3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE
| Applicant | 3t Medical Systems, LLC, Conifer CO, US |
| Decision | Substantially Equivalent, May 3, 2002 |
| Received | Feb 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020365
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.