First Source, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
First Source, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iQFlex Pro, iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System, I-Q View
3
Total
3
Cleared
0
Denied
First Source, Inc. has 3 FDA 510(k) cleared medical devices. Based in Rochester, US.
Latest FDA clearance: Jul 2024. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by First Source, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medmonts Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - First Source, Inc.
3 devices