510(k) K842039 ยท KNZ Accessories, A-V Shunt
ARGON DUAL LUMEN HEMODIALYSIS, CATHETER
| Applicant | Argon Medical Corp., Athens TX, US |
| Decision | Substantially Equivalent, Jan 29, 1985 |
| Received | May 21, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842039
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.