510(k) K891688 ยท HCG Device, Neurovascular Embolization
COIL AND COIL DELIVERY SYSTEM
| Applicant | Target Therapeutics, San Jose CA, US |
| Decision | Substantially Equivalent, Sep 22, 1989 |
| Received | Mar 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891688
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.