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510(k) K240189

NM-01/CPT neurometer (NM-01/CPT) by Mde Orvosbiológiai Kutató, Fejleszto, — Product Code JXE

K240189 is an FDA 510(k) premarket notification submitted by Mde Orvosbiológiai Kutató, Fejleszto, for the device "NM-01/CPT neurometer (NM-01/CPT)". The FDA issued a decision of Substantially Equivalent on March 26, 2025. The device falls under product code JXE (Device, Nerve Conduction Velocity Measurement), a Class II device regulated under 21 CFR 882.1550.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 26, 2025
Date Received
January 24, 2024
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

Other clearances for product code JXE

  • K190536 — Mediracer NCS (September 25, 2019)
  • K070109 — NEUROMETRIX ADVANCE (April 25, 2008)
  • K060584 — NC-STAT (July 31, 2006)
  • K053058 — XLTEK NEUROPATH, MODEL PK1070 (February 7, 2006)
  • K052904 — VIRTUAL MEDICAL SYSTEMS MODEL VT3000 (October 27, 2005)
  • K041320 — MODIFICATION TO NC-STAT (August 12, 2004)
  • K013459 — MODIFICATION OF NC-STAT (January 17, 2002)
  • K012069 — MODIFICATION TO:BREVIO NERVE CONDUCTION TEST INSTRUMENT (August 1, 2001)
  • K003508 — NC-STAT (January 17, 2001)
  • K001692 — NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8 (November 24, 2000)

FDA data resources