510(k) K051814 ยท FIE Needle, Fistula
JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
| Applicant | Jms North America Corp., Hayward CA, US |
| Decision | Substantially Equivalent, Aug 4, 2005 |
| Received | Jul 5, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051814
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.