510(k) K884375 ยท DQR Cannula, Catheter
TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
| Applicant | Argon Medical Corp., Athens TX, US |
| Decision | Substantially Equivalent, Jan 11, 1989 |
| Received | Oct 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884375
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.