510(k) K053058
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