510(k) K801211 ยท FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
COBE HEMOFLO BLOOD TUBING SETS
| Applicant | Cobe Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 14, 1980 |
| Received | May 20, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801211
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.