510(k) K001678 ยท HCG Device, Neurovascular Embolization
PVA FOAM EMBOLIZATION PARTICLES
| Applicant | Surgica Corp., El Dorado Hills CA, US |
| Decision | Substantially Equivalent, Jan 25, 2001 |
| Received | Jun 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001678
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.