Cedars-Sinai Medical Center is one of 18385 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cedars-Sinai Medical Center - FDA 510(k) Cleared Devices
Recent clearances: CSMC Cardiac Suite, CEDARS-SINAI CARDIAC SUITE NUCLEAR MEDICINE SOFTWARE, CEDARS-SINAI CARDIAC SUITE NUCLEAR MEDICINE SOFTWARE
Cedars-Sinai Medical Center, is a health sciences organization with a manufacturing facility in Jacksonville, US. The organization has developed and cleared medical devices primarily in the Radiology sector.
The company received 5 FDA 510(k) clearances from 5 total submissions between 2011 and 2017. All submissions focused on Radiology devices, reflecting the organization's specialization in cardiac imaging and nuclear medicine software applications. The company is currently inactive, with no clearances recorded in the past five years.
Historical cleared devices include the CSMC Cardiac Suite and related nuclear medicine software platforms. These products supported cardiac imaging workflows and diagnostic capabilities. For detailed information on specific device names, product codes, and clearance dates, explore the complete regulatory record.