Koios DS (3.8)
Koios Medical, Inc. · K253884
FDA-authorized Predetermined Change Control Plan
- Company
- Koios Medical, Inc.
- 510(k)/De Novo #
- K253884
- Decision date
- 2026-07-02
- Panel
- Radiology
- Pathway
- 510(k)
- Category
- AI/SaMD
- PCCP type
- Retraining
- Monitoring commitment
- Not stated
What this PCCP covers. Permits model retraining with additional data
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- K261085Rapid Vessel Occlusion (Rapid VO)iSchemaview2026-07-13AI/SaMDRetraining
- K260973InferOperate SuiteBeijing Infervision Healthcare Medical Technology Co., Ltd.2026-07-07AI/SaMDRetraining
- K260714MammoScreen® (5)Therapixel2026-06-26AI/SaMDCompatibility expansion
Want the monitoring teardown?
We read the PCCP for Koios DS (3.8), then map the post-market monitoring that its modification protocol requires, including the deployment-period evidence most teams can't reconstruct at modification time. Sentir is the independent system of record that produces it.
Book a callSource: U.S. FDA public records (openFDA 510(k)/De Novo databases and accessdata.fda.gov). PCCP type and category are editorial classifications based on public documents, not official FDA designations.
This page is a factual summary of public FDA records. Sentir Health is not affiliated with or endorsed by the named companies or the U.S. Food and Drug Administration. Spot an error? Request a correction.