510(k) K110157

SYSLOC MINI V3 by JMS North America Corporation — Product Code FIE

K110157 is an FDA 510(k) premarket notification submitted by JMS North America Corporation for the device "SYSLOC MINI V3". The FDA issued a decision of Substantially Equivalent on February 11, 2011. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. JMS North America Corporation has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 11, 2011
Date Received
January 19, 2011
Clearance Type
Special
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