510(k) K093637 ยท FIE Needle, Fistula
JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300
| Applicant | Jms North America Corp., Crofton MD, US |
| Decision | Substantially Equivalent, Feb 9, 2010 |
| Received | Nov 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093637
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.