510(k) K960047 ยท FMF Syringe, Piston
BRANNON PEDI PORTSYRINGE
| Applicant | James K. Brannon, Culver City CA, US |
| Decision | Substantially Equivalent, May 24, 1996 |
| Received | Jan 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960047
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.