510(k) K861860 ยท KRL Detector, Bubble, Cardiopulmonary Bypass
COBE ACCESSORY INTERFACE MODULE (AIM)
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Jul 18, 1986 |
| Received | May 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861860
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.