510(k) K071307 ยท FMI Needle, Hypodermic, Single Lumen
INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003
| Applicant | Inviro Medical Devices, Inc., Duluth GA, US |
| Decision | Substantially Equivalent, Feb 12, 2008 |
| Received | May 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071307
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.