510(k) K123710 ยท FMF Syringe, Piston
UNITOX BOTOX SYRINGE
| Applicant | Bio-Med USA, Inc., Paterson NJ, US |
| Decision | Substantially Equivalent, May 9, 2013 |
| Received | Dec 4, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123710
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.