510(k) K904849 ยท FHO Pneumoperitoneum Needle
ORIGINEEDLE(TM)
| Applicant | Origin Medsystems, Inc., San Mateo CA, US |
| Decision | Substantially Equivalent, Mar 29, 1991 |
| Received | Oct 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904849
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.