510(k) K962999 ยท EJI Syringe, Cartridge
SAFETY INJECTION SYSTEM
| Applicant | Integritech, Inc., Mobile AL, US |
| Decision | Substantially Equivalent, Jan 22, 1997 |
| Received | Aug 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962999
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.