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Scrape FDA 510(k) Device Clearances (Medtronic)

Pull FDA 510(k) clearances for a device manufacturer by applicant name and product code, with decision date and outcome plus a verify link.

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Clinical Trials & FDA Pipeline Intelligence Scraper
Clinical Trials & FDA Pipeline Intelligence Scraperconstructive_calm/clinical-trials-fda-scraper
ID
Path
Device
Applicant
+4 fields
Text
Number
Boolean
List
Object

Input

Scraping mode(required):device_clearances
Applicant name (device_clearances mode):Medtronic
FDA product code (3-letter code):DXN
Device pathways:510k
Max items:25

Output fields

ID
Path
Device
Applicant
Code
Decision
Outcome
FDA

How it works

Sign up on Apify or log in

The Clinical Trials & FDA Pipeline Intelligence Scraper Actor is ready to run with the inputs already set for "Scrape FDA 510(k) Device Clearances (Medtronic)". Sign up or log in and you'll land in Apify Console with a copy of this exact task.

Start the "Scrape FDA 510(k) Device Clearances (Medtronic)" task

The Clinical Trials & FDA Pipeline Intelligence Scraper Actor will start running based on the input automatically. You can also change all the input fields, like scraping mode, applicant name (device_clearances mode), and more, to match your specific use case.

Receive the "Scrape FDA 510(k) Device Clearances (Medtronic)" output

Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as ID, path, device, and more.

Integrate into your workflow

The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "Scrape FDA 510(k) Device Clearances (Medtronic)" task via API.

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