510(k) K070384 ยท KRA Catheter, Continuous Flush
ARGON CONTINUOUS FLUSH DEVICE
| Applicant | Argon Medical Devices, Inc., Athens TX, US |
| Decision | Substantially Equivalent, Mar 29, 2007 |
| Received | Feb 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070384
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.