510(k) K020047 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
RUBICOR BREAST BIOPSY DEVICE
| Applicant | Rubicor Medical, Inc., San Carlos CA, US |
| Decision | Substantially Equivalent, Apr 5, 2002 |
| Received | Jan 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020047
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 11, 2006 | Rubicor Medical Rubicor EnCapsule Breast Biopsy Device, Part Number 31358,
Product is manufactured and distributed by Rubicor Medical, Inc., 600 Chesapeake Dr., Redwood City, CA 94063 Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.