510(k) K070449 ยท KNT Tubes, Gastrointestinal (And Accessories)
LUMILOC (TM) SAFETY INTRODUCER NEEDLE
| Applicant | Specialized Health Products International, Inc., Salt Lake UT, US |
| Decision | Substantially Equivalent, Jun 14, 2007 |
| Received | Feb 15, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070449
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.