510(k) clearances in the last 90 days
Devices cleared for US market through the 510(k) pathway in the last quarter, with review times.
openFDA Scraper · Drug Events, Recalls, Labels & Devicesreapx/openfda-scraper
Record ID
Primary date
Device name
Applicant
+6 fieldsTextNumberBooleanListObject
Input
FDA dataset:device-510k-clearances
Max records:400
In the last N days:90
Output fields
Record ID
Primary date
Device name
Applicant
Decision
Clearance type
Advisory committee
Product code
Review days
State
Sign up on Apify01
Create your Apify account to access the openFDA Scraper · Drug Events, Recalls, Labels & Devices.
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.
