510(k) K963307 ยท HCG Device, Neurovascular Embolization
GDC PATIENT RETURN ELECTTRODE MODEL 45021
| Applicant | Target Therapeutics, Freemont CA, US |
| Decision | Substantially Equivalent, Dec 17, 1996 |
| Received | Aug 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963307
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.