Inspirstar, Inc. is one of 24231 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inspirstar, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INSPIRSTAR GLOVE ELECTRODE, INSPIRSTAR IS02 MICROCURRENT STIMULATOR
2
Total
2
Cleared
0
Denied
Inspirstar, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chandler, US.
Historical record: 2 cleared submissions from 2006 to 2006. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Inspirstar, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Inspirstar, Inc.
2 devices