510(k) K001251 ยท DQX Wire, Guide, Catheter
SNIPER, MODEL OR-3872XX SERIES
| Applicant | Nipro Medical Corp., Athens TX, US |
| Decision | Substantially Equivalent, Jul 7, 2000 |
| Received | Apr 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001251
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 25, 2012 | Nipro Medical Corporation AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Regular.
AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional devi Terminated |
DQX | None listed |
| Oct 25, 2012 | Nipro Medical Corporation AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Stiff.
AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional device Terminated |
DQX | None listed |
| Oct 25, 2012 | Nipro Medical Corporation AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Regular.
AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional d Terminated |
DQX | None listed |
| Oct 25, 2012 | Nipro Medical Corporation AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Stiff.
AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional dev Terminated |
DQX | None listed |
| Oct 25, 2012 | Nipro Medical Corporation AquaLiner Hydrophilic Guidewire 0.035" X 180cm, Angle / Regular.
AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional dev Terminated |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.