510(k) K010692 ยท FMF Syringe, Piston
THE WAND PLUS COMPUTER CONTROLLED ANESTHETIC DELIVERY SYSTEM
| Applicant | Spintech, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 29, 2001 |
| Received | Mar 8, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010692
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.