510(k) K002813

NIPRO SAFETOUCH SAFETY FISTULA NEEDLE by Nipro Medical Corp. — Product Code FIE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 2000
Date Received
September 8, 2000
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