510(k) K052578 ยท DTK Filter, Intravascular, Cardiovascular
BARD G2 FILTER SYSTEM - JUGULAR/SUBCLAVIAN DELIVERY KIT, MODEL RF-320J
| Applicant | Bard Peripheral Vascular, Inc., Tempe AZ, US |
| Decision | Unknown, Nov 25, 2005 |
| Received | Sep 20, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052578
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 1, 2007 | Bard Peripheral Vascular Inc G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-320J Terminated |
DTK | None listed |
| Feb 1, 2007 | Bard Peripheral Vascular Inc Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-220J ***For Canada & Australia only*** Terminated |
DTK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.