510(k) K072602 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM
| Applicant | Medpro Safety Products, Inc., Lexington KY, US |
| Decision | Substantially Equivalent, Jun 18, 2008 |
| Received | Sep 14, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K072602
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.