510(k) K011103

BD SPRING BASED SYRINGE by Bd — Product Code MEG

K011103 is an FDA 510(k) premarket notification submitted by Bd for the device "BD SPRING BASED SYRINGE". The FDA issued a decision of Substantially Equivalent on June 13, 2001. The device falls under product code MEG (Syringe, Antistick), a Class II device regulated under 21 CFR 880.5860. Bd has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 2001
Date Received
April 11, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Antistick
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type