BD Preset and BD A-Line Arterial Blood Collection Syringes
Summary
Becton, Dickinson and Company received 510(k) clearance for BD Preset and BD A-Line Arterial Blood Collection Syringes, a JKA device. Cleared on 2026-04-15.
Details
Source
510(k) Clearance
External ID
K260128
Action Date
2026-04-15
Status
Special
Category
device
Product Code
JKA
Product Description
BD Preset and BD A-Line Arterial Blood Collection Syringes. Product code: JKA.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 413 device clearances issued this month. Becton, Dickinson and Company has received 51 total clearances in our database.
Becton, Dickinson and Company has 54 FDA actions in our database, including 3 recalls and 51 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 Becton, Dickinson and Company have FDA actions?
Becton, Dickinson and Company has 54 FDA actions in our database, including 3 recalls and 51 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K260128" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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