510(k) K955293 ยท KRD Device, Vascular, For Promoting Embolization
FIBERED PLATINUM COIL, .035 TYPE
| Applicant | Target Therapeutics, Freemont CA, US |
| Decision | Substantially Equivalent, Feb 6, 1996 |
| Received | Nov 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955293
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 19, 2003 | Boston Scientific Corporation Fibered Platinum Coil, 0.035 Type,
4 mm x 30 mm
Catalog no. 372403 Terminated |
None listed | |
| Jul 19, 2003 | Boston Scientific Corporation Fibered Platinum Coil, 0.035 Type,
9 mm x 60 mm
Catalog no. 372906 Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.