510(k) K884375

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER by Argon Medical Corp. — Product Code DQR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 1989
Date Received
October 18, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cannula, Catheter
Device Class
Class II
Regulation Number
870.1300
Review Panel
CV
Submission Type