Microhelix, Inc. is one of 25138 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microhelix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MHLX7EC TRANSDUCER
1
Total
1
Cleared
0
Denied
Microhelix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bainbridge Island, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Microhelix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microhelix, Inc.
1 devices