510(k) K102010 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET
| Applicant | Medpro Safety Products, Inc., Lake Bluff IL, US |
| Decision | Substantially Equivalent, Nov 19, 2010 |
| Received | Jul 16, 2010 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K102010
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.