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., Philips Medical Systems Nederland B.V. and Ziehm Imaging GmbH.
325
Total
325
Cleared
113d
Avg days
1991
Since
325 devices
Cleared
Aug 19, 1996
PHILIPS MULTIDIAGNOST 4
Philips Medical Systems, Inc.
Radiology
132d
Cleared
May 20, 1996
CLINIX MP
Philips Medical Systems (Cleveland), Inc.
Radiology
75d
Cleared
Apr 29, 1994
PHILIPS DCI-SX
Philips Medical Systems, Inc.
Radiology
777d
Cleared
Mar 16, 1994
TC+ SYSTEM (TILTING C-ARM SYSTEM)
GE Medical Systems
Radiology
79d
Cleared
Sep 15, 1992
UROSKOP D1, UROSKOP D2, AND UROSKOP D3
Siemens Medical Solutions USA, Inc.
Radiology
83d
Cleared
Aug 28, 1991
CSP
Fischer Imaging Corp.
Radiology
86d