Home › Device types › DQT
Occluder, Catheter Tip
FDA product code DQT · Class 2 · Cardiovascular
8
Registered devices
153
Adverse events
4
Recalls
12
510(k) clearances
Devices with this code
Pruitt Irrigation Occlusion Catheter — Lemaitre Vascular, Inc.Polyurethane Dual Lumen Occlusion Catheter — Lemaitre Vascular, Inc.Polyurethane Dual Lumen Occlusion Catheter — Lemaitre Vascular, Inc.Pruitt Aortic Occlusion Catheter — Lemaitre Vascular, Inc.Pruitt Aortic Occlusion Catheter — Lemaitre Vascular, Inc.Pruitt Irrigation Occlusion Catheter — Lemaitre Vascular, Inc.Polyurethane Dual Lumen Occlusion Catheter — Lemaitre Vascular, Inc.Polyurethane Dual Lumen Occlusion Catheter — Lemaitre Vascular, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-11 | LeMaitre Vascular, Inc. | During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier). |
| 2013-10-21 | Medtronic Vascular | Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire. |
| 2013-10-21 | Medtronic Vascular | Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire. |
| 2005-05-17 | LeMaitre Vascular, Inc. | LeMaitre Vascular is recalling certain lots of its Pruitt Aortic Occlusion Catheters due to a packaging defect which could compromise product sterility. |
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