ClearanceBrief
510(k) K120613 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

OEC 9900 ELITE

ApplicantGe Healthcare Surgery GE Oec Medical Systems, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Apr 6, 2012
ReceivedFeb 29, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120613

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
Aug 27, 2020Ge Healthcare
The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include chola
Open, Classified
RCCNone listed
Jan 20, 2017GE OEC Medical Systems, Inc
OEC 9900 Elite. MDL Numbers: D148942, D155043
Terminated
OWBNone listed
Jan 9, 2017GE OEC Medical Systems, Inc
The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical appli
Terminated
OXONone listed

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