510(k) K002181 ยท HCG Device, Neurovascular Embolization
GDC ULTRASOFT COIL
| Applicant | Boston Scientific, Target, Fremont CA, US |
| Decision | Substantially Equivalent, Aug 11, 2000 |
| Received | Jul 19, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K002181
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.