Constat MCP — FDA Device Evidence Lifecycle

FDA and CMS evidence for AI medical devices: 510(k), postmarket, reimbursement, and compliance.

Description supplied by the publisher; it is a claim, not verified evidence.

Name
com.healthai/radar
Listed in
Official MCP Registry
Publisher
healthai-hq (verified publisher)
Latest version
0.5.3
Published
2026-07-30
Evidence
Analyzed by UND Assay

Source: https://github.com/healthai-hq/fda-risk-radar

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