510(k) K213156

BD Nano 2nd Gen Pen Needle by Becton, Dickinson And Company — Product Code FMI

K213156 is an FDA 510(k) premarket notification submitted by Becton, Dickinson And Company for the device "BD Nano 2nd Gen Pen Needle". The FDA issued a decision of Substantially Equivalent on Dec 8, 2021. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Becton, Dickinson And Company has 329 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 8, 2021
Date Received
Sep 20, 2021
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Hypodermic, Single Lumen
Device Class
Class II
Regulation Number
880.5570
Review Panel
HO
Submission Type
510(k)