510(k) K012917 ยท HFW Clamp, Umbilical
DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
| Applicant | Dynarex Corp., Maineville OH, US |
| Decision | Substantially Equivalent, Nov 28, 2001 |
| Received | Aug 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012917
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.