ClearanceBrief
510(k) K073543 ยท OWB Interventional Fluoroscopic X-Ray System

OEC 9900 ELITE

ApplicantGe Oec Medical Systems, Salt Lake City UT, US
DecisionSubstantially Equivalent, May 2, 2008
ReceivedDec 17, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073543

DateFirm and productCodeLinked 510(k)
Aug 22, 2025GE Medical Systems, LLC
GE HealthCare OEC 9900 Elite C-arm Systems.
Open, Classified
OWBNone listed
Dec 18, 2024GE OEC Medical Systems, Inc
OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnost
Open, Classified
OXONone listed
Jul 31, 2023GE OEC Medical Systems, Inc
OEC 9900 Systems with 9-inch Image Intensifier
Open, Classified
OXONone listed
Jul 31, 2023GE OEC Medical Systems, Inc
Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER, 9 INCH, TOSHIBA; P/N 5761613 SERVICE PART, IMAGE INTENSIFIER, 9 INCH - used with OEC Flexiview 8800,
Open, Classified
OXONone listed
Apr 16, 2014GE OEC Medical Systems, Inc
The OEC 9900 Elite mobile fluoroscopy system (image intensified fluoroscopic x-ray) is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventiona
Terminated
OWBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.