510(k) K260128

Device
BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes
Applicant
Becton, Dickinson and Company
510(k) number
K260128
Product code
JKA
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-15
Date received
2026-01-16
Regulation
862.1675
Classification name
Tubes, Vials, Systems, Serum Separators, Blood Collection
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Sharanya Jangiti
Address
1 Becton Dr. Franklin Lakes NJ US 07417 07417

FDA Registration Numbers

Source Documents

510(k) summary PDF

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