Blue Spark Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blue Spark Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TempTraq
2
Total
2
Cleared
0
Denied
Blue Spark Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Westlake, US.
Historical record: 2 cleared submissions from 2015 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Blue Spark Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Blue Spark Technologies, Inc.
2 devices