United States·health

US openFDA — Medical device 510(k) clearances

FDA 510(k) premarket notification clearances for medical devices: K-number, applicant, device name, advisory committee, decision, and dates. Aggregate public data from openFDA.

us_openfda_device_510k230,000 recordsCachedCached endpoint

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FDA 510(k) premarket notification clearances for medical devices: K-number, applicant, device name, advisory committee, decision, and dates. Aggregate public data from openFDA.

Record count
230,000 records
Source type
Cached endpoint
Last refreshed
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Group
Healthcare Regulatory

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