510(k) K992404 ยท FMF Syringe, Piston
THE WAND
| Applicant | Spintech, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 6, 2000 |
| Received | Jul 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992404
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.