510(k) K023218

MODIFICATION TO PLEXOLONG SETS by Pajunk GmbH — Product Code BSP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 24, 2003
Date Received
September 26, 2002
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
Device Class
Class II
Regulation Number
868.5150
Review Panel
AN
Submission Type