510(k) K991404 ยท FMI Needle, Hypodermic, Single Lumen
PLATYPUS AV FISTULA NEEDLE PROTECTOR (AVFNP)
| Applicant | Itl Corporation Pty, Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, May 14, 1999 |
| Received | Apr 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991404
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.