510(k) K082882

A.V. FISTULA BLUNT NEEDLE SET by Jms North America Corp. — Product Code FIE

K082882 is an FDA 510(k) premarket notification submitted by Jms North America Corp. for the device "A.V. FISTULA BLUNT NEEDLE SET". The FDA issued a decision of Substantially Equivalent on January 21, 2009. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Jms North America Corp. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 2009
Date Received
September 30, 2008
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