510(k) K970962

JMS AV FISTULA NEEDLE by Jms Co., Ltd. — Product Code FIE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1997
Date Received
March 17, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Fistula
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type