510(k) K032899 ยท DQX Wire, Guide, Catheter
RADIUS COUGAR WIRE
| Applicant | Radius Medical Technologies, Inc., Hopkonton MA, US |
| Decision | Substantially Equivalent, Oct 17, 2003 |
| Received | Sep 17, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032899
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 15, 2013 | Medtronic Vascular Cougar Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ, CGRXT190HS, CGRXT190J, CGRXT190S, CGRXT300HJ, CGRXT300HS, CGRXT300J, CGRXT300S
Medtr Terminated |
DQX | None listed |
| Nov 15, 2013 | Medtronic Vascular COUGAR Steerable Guidewire; Models: LVCLS190J, LVCLS190S, LVCXT190J, LVCXT190S
Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or inter Terminated |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.