Icubate, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Icubate, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iC-GN iC-Cassette for use on the iC-System
2
Total
2
Cleared
0
Denied
Icubate, Inc. has 2 FDA 510(k) cleared medical devices. Based in Huntsville, US.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Icubate, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MDC Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Icubate, Inc.
2 devices