Medical Device Manufacturer · US , Seattle , WA

Measure Labs, Inc. (Dba Preemptiveai, Inc.) - FDA 510(k) Cleared Devi...

1 submissions · 1 cleared · Since 2026

Total

Cleared

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

1-1 of 1

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

RQM+

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026