510(k) K772362 ยท FIE Needle, Fistula
AVF SET FOR SINGLE NEEDLE HEMODIALYSIS
| Applicant | Terumo America, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 17, 1978 |
| Received | Dec 27, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772362
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.