OWB · Class II · 21 CFR 892.1650

FDA Product Code OWB: Interventional Fluoroscopic X-ray System

Under FDA product code OWB, interventional fluoroscopic X-ray systems are cleared for real-time image guidance during minimally invasive procedures.

These systems provide continuous or pulsed X-ray imaging to guide catheters, wires, and implants during cardiovascular, neurological, and orthopedic interventions. Advanced systems include flat panel detectors, 3D roadmapping, and dose management software.

OWB devices are Class II medical devices, regulated under 21 CFR 892.1650 and reviewed by the FDA Radiology panel.

Leading manufacturers include Siemens Medical Solutions USA, Inc., Ziehm Imaging GmbH and Canon Medical Systems Corporation.

319
Total
319
Cleared
112d
Avg days
1991
Since
319 devices
217–240 of 319
No devices found for this product code.