510(k) K081694 ยท EJI Syringe, Cartridge
DENJECTOR
| Applicant | Dxm Co., Ltd., Great Neck NY, US |
| Decision | Substantially Equivalent, Sep 12, 2008 |
| Received | Jun 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081694
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.