510(k) K882221 ยท DYB Introducer, Catheter
OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
| Applicant | Argon Medical Corp., Athens TX, US |
| Decision | Substantially Equivalent, Aug 12, 1988 |
| Received | May 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882221
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.