510(k) K182320

BD Contoured Base Pen Needle by Becton, Dickinson And Company — Product Code FMI

K182320 is an FDA 510(k) premarket notification submitted by Becton, Dickinson And Company for the device "BD Contoured Base Pen Needle". The FDA issued a decision of Substantially Equivalent on Dec 20, 2018. 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 20, 2018
Date Received
Aug 27, 2018
Clearance Type
Traditional
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)