Cardica, Inc. is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardica, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dextera MicroCutter 5/80 Blue Reload, Dextera MicroCutter 5/80 Blue Curved Tip Reload, MicroCutter XCHANGE 30 Stapler, MicroCutter XCHANGE 30 Blue Cartridge, MicroCutter XCHANGE 30 White Cartridge, MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 BLUE CARTRIDGE
Cardica, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Redwood City, US.
Historical record: 15 cleared submissions from 2005 to 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.