510(k) K961457 ยท EJI Syringe, Cartridge
SUBLIMINATOR
| Applicant | Healex Products, Inc., Providence RI, US |
| Decision | Substantially Equivalent, Jul 18, 1996 |
| Received | Apr 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961457
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.