Measure Labs, Inc. (Dba Preemptiveai, Inc.)
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- Devices
- 1
What Measure Labs, Inc. (Dba Preemptiveai, Inc.) makes
Measure Labs, Inc. develops the PreemptiveAI Clinical SDK, a software tool designed for clinical applications to support predictive analytics and decision-making in healthcare settings.
The PreemptiveAI Clinical SDK is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
PreemptiveAI Clinical SDK Ref K250233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Measure Labs, Inc. (Dba Preemptiveai, Inc.) have in the registry?
The registry currently lists 1 device for Measure Labs, Inc. (Dba Preemptiveai, Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Measure Labs, Inc. (Dba Preemptiveai, Inc.)'s devices?
Among its 1 most recently registered device, Measure Labs, Inc. (Dba Preemptiveai, Inc.) has devices listed in FDA 510(k) (1 device).
What risk classes do Measure Labs, Inc. (Dba Preemptiveai, Inc.)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Measure Labs, Inc. (Dba Preemptiveai, Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Measure Labs, Inc. (Dba Preemptiveai, Inc.) in the registry?
The most recently registered devices listed for Measure Labs, Inc. (Dba Preemptiveai, Inc.) include PreemptiveAI Clinical SDK.