510(k) K972511 ยท DXE Catheter, Embolectomy
AMPLATZ GOOSE NECK SNARE KIT/ CATHETER
| Applicant | Microvena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, Mar 6, 1998 |
| Received | Jul 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972511
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 11, 2007 | Ev3, Inc Amplatz Goose Neck Snare Kit, 6 Fr, Lot 1650307, REF: GN3000, Use By 2009-09-01, Sterile EO
ev3 4600 Nathan Lane North, Plymouth, MN 55442-2920 USA
THE ENDOVASCULAR COMPANY.
The Snare Kit contains Terminated |
DXE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.