510(k) K013040 ยท MDM Instrument, Manual, Surgical, General Use
LIGHT SABER INTRODUCER NEEDLE
| Applicant | Minrad, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Dec 7, 2001 |
| Received | Sep 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013040
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.