FDA 510(k) device clearances decided this year
Reads openFDA’s device/510k dataset for clearances with a decision date in 2026 and returns 100 rows: the K number, device name, applicant, decision date and decision code, product code, advisory committee, clearance type, and the applicant’s city and state, with the trimmed source record kept in raw. Change the date window, or add device/pma for premarket approvals. $0.30 per 1,000 FDA records.
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