510(k) K771209 ยท FMI Needle, Hypodermic, Single Lumen
TERUFUSION BLOOD ADMIN. SET
| Applicant | Terumo America, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 26, 1977 |
| Received | Jul 5, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771209
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.