Amplatzer TorqVue Delivery System
Summary
Abbott received 510(k) clearance for Amplatzer TorqVue Delivery System, a DQY device. Cleared on 2026-04-24.
Details
Source
510(k) Clearance
External ID
K260993
Action Date
2026-04-24
Status
Special
Category
device
Product Code
DQY
Product Description
Amplatzer TorqVue Delivery System. Product code: DQY.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Abbott has received 6 total clearances in our database.
Abbott has 21 FDA actions in our database, including 15 recalls and 6 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Abbott have FDA actions?
Abbott has 21 FDA actions in our database, including 15 recalls and 6 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K260993" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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