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.
Input
Output fields
Sign up on Apify01
Create your Apify account to access the Clinical Trials & FDA API — ClinicalTrials.gov + openFDA.
Start the run02
The Actor will start running based on the input automatically.
Receive the output03
Monitor the progress in real-time. You will be notified as soon as your dataset is complete and ready for review.
Integrate into your workflow04
The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow.
