510(k) K111424 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM TUBE-TOUCH
| Applicant | Medpro Safety Products, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Jul 29, 2011 |
| Received | May 23, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111424
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.