510(k) K053058

XLTEK NEUROPATH, MODEL PK1070 by Excel Tech. , Ltd. — Product Code JXE

K053058 is an FDA 510(k) premarket notification submitted by Excel Tech. , Ltd. for the device "XLTEK NEUROPATH, MODEL PK1070". The FDA issued a decision of Substantially Equivalent on February 7, 2006. The device falls under product code JXE (Device, Nerve Conduction Velocity Measurement), a Class II device regulated under 21 CFR 882.1550. Excel Tech. , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 2006
Date Received
October 31, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Nerve Conduction Velocity Measurement
Device Class
Class II
Regulation Number
882.1550
Review Panel
NE
Submission Type