510(k) K900723 ยท HCG Device, Neurovascular Embolization
ITC BUNJI COIL
| Applicant | Interventional Therapeutics Corp., South San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 19, 1991 |
| Received | Feb 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900723
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.