AuST Steerable Sheath
Summary
CenterPoint Systems, LLC received 510(k) clearance for AuST Steerable Sheath, a DYB device. Cleared on 2026-04-07.
Details
Source
510(k) Clearance
External ID
K260942
Action Date
2026-04-07
Status
Special
Category
device
Product Code
DYB
Product Description
AuST Steerable Sheath. Product code: DYB.
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. CenterPoint Systems, LLC has received 13 total clearances in our database.
CenterPoint Systems, LLC has 13 FDA actions in our database, including 13 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 CenterPoint Systems, LLC have FDA actions?
CenterPoint Systems, LLC has 13 FDA actions in our database, including 0 recalls and 13 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K260942" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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