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FDA AI/ML Software as a Medical Device Action Plan + 510(k) + PMA + De Novo pathways for US MedTech and digital health firms.

Project description

mcp-name: io.github.CSOAI-ORG/fda-samd-mcp

FDA AI/ML SaMD Compliance MCP

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PyPI License: MIT MEOK AI Labs

FDA AI/ML Software as a Medical Device Action Plan + 510(k) + PMA + De Novo pathways for US MedTech and digital health firms.

Install

pip install fda-samd-mcp

Tools

Tool Purpose
classify_sw_device FDA SaMD vs SiMD classification + IMDRF risk framework
regulatory_pathway 510(k) / De Novo / PMA pathway selection
pccp_template Predetermined Change Control Plan generator (locked vs adaptive AI)
good_ml_practice FDA Good Machine Learning Practice (GMLP) 10 principles
ai_ml_action_plan FDA AI/ML Action Plan focus area assessment

Pairs with

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  • Other MEOK governance MCPs via SOV3 mcp_bridge_call

Pricing

  • Free: 10 calls/day. No API key required.
  • Pro £79/mo: unlimited + signed attestations. Subscribe
  • Enterprise £1,499/mo: white-label + on-premise + SLA. hello@meok.ai

Status

Scaffold v1.0.0 ships the MCP framework + 5 tool stubs. v1.1.0 will add real regulation data ingestion.

If your team needs this MCP fully-loaded faster, ping hello@meok.ai for sponsored development.

License

MIT © MEOK AI Labs

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