Medical Device Manufacturer · US , San Diego , CA

Carefusion 303, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2011

Total

Cleared

Denied

Carefusion 303, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Apr 2025. Active since 2011. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Carefusion 303, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Carefusion 303, Inc. is one of 16115 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Carefusion 303, Inc.

7 devices

1-7 of 7