Home › AVINGER, INC. › Ocelot IV
Ocelot IV
AVINGER, INC. · Model O250 · UDI-DI 00851354004233
PDU
Prescription
1
510(k) clearances
1,386
Adverse events (2 deaths)
7
Recalls
41
Facilities
Description
The Ocelot System is intended to facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention using OCT-assisted orientation and imaging. The system is an adjunct to fluoroscopy by providing images of vessel lumen and wall structures. The Ocelot System is contraindicated for use in the iliac, coronary, cerebral, renal or carotid vasculature.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-11-14 | Bard Peripheral Vascular Inc | Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart require |
| 2020-10-16 | Ra Medical Systems, Inc. | Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' po |
| 2020-07-24 | Ra Medical Systems, Inc. | Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury. |
| 2020-01-23 | Ra Medical Systems, Inc. | A software issue was identified which could result in user or patient injury, or may adversely impact laser performance. It is possible that an unintended release of laser light (r |
| 2019-09-19 | Ra Medical Systems, Inc. | The firm has become aware there is a potential problem with its DABRA catheters resulting in higher catheter calibration failure rate due to the product shelf life is currently les |
| 2018-02-15 | Ra Medical Systems Inc | Lasers/Catheters did not calibrate during set-up prior to use. |
| 2015-07-22 | Volcano Corporation | Due to a manufacturing defect, there is the possibility that a small wire could extend through the catheter shaft of the Pioneer Plus intravascular Ultrasound Guided Re-Entry Cathe |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.