Mauna Kea Technologies, Inc. is one of 24579 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mauna Kea Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CELLVIZIO 100 SERIES SYSTEM WITH CONFOCAL MINIPROBES
1
Total
1
Cleared
0
Denied
Mauna Kea Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Newton, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mauna Kea Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mauna Kea Technologies, Inc.
1 devices