Measure Labs, Inc. (Dba Preemptiveai, Inc.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Measure Labs, Inc. (Dba Preemptiveai, Inc.) - FDA 510(k) Cleared Devi...
Recent clearances: PreemptiveAI Clinical SDK
1
Total
1
Cleared
0
Denied
Measure Labs, Inc. (Dba Preemptiveai, Inc.) has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Measure Labs, Inc. (Dba Preemptiveai, Inc.) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Measure Labs, Inc. (Dba Preemptiveai, Inc.)
1 devices