510(k) K930091 ยท DQX Wire, Guide, Catheter
CORDIS REFLEX STEERABLE GUIDEWIRE
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Apr 7, 1993 |
| Received | Jan 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930091
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 9, 2006 | Cordis Corporation CORDIS SV-5 Steerable Guidewire, 180 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company, ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA, Catalog # 503558. Terminated |
DXQ | None listed |
| Sep 9, 2006 | Cordis Corporation CORDIS-SV-5 Steerable Guidewire, 300 cm.,5 Steerable Guidewires,Cordis a Johnson Johnson Company ,ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA., Catalog # 503558X Terminated |
DXQ | None listed |
| Sep 9, 2006 | Cordis Corporation CORDIS SV-8 Steerable Guidewire, 180 cm. , 5 Steerable Guidewires, Cordis a Johnson Johnson Company, ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA., Catalog # 503658 Terminated |
DXQ | None listed |
| Sep 9, 2006 | Cordis Corporation CORDIS SV-8 Steerable Guidewire, 300 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA, Catalog # 503658X Terminated |
DXQ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.