510(k) K855066 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
SWANK ARTERIAL LINE BLOOD FILTER HF6000
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Feb 26, 1986 |
| Received | Dec 18, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855066
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.