Accelerate Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accelerate Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Accelerate Arc System, Accelerate Pheno System, Accelerate PhenoTest BC Kit
2
Total
2
Cleared
0
Denied
Accelerate Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Tucson, US.
Latest FDA clearance: Sep 2024. Active since 2020. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Accelerate Diagnostics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Precision For Medicine, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Accelerate Diagnostics, Inc.
2 devices