510(k) K121270 ยท KZE Injector, Fluid, Non-Electrically Powered
BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
| Applicant | Bioject Medical Technologies, Inc., Tigard OR, US |
| Decision | Substantially Equivalent, Jul 19, 2012 |
| Received | Apr 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121270
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.