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510(k) K252951

Genesis Sleep by Neurofield, Inc. — Product Code QJQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 31, 2025
Date Received
September 16, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety
Device Class
Class II
Regulation Number
882.5800
Review Panel
NE
Submission Type

To provide electrical current to the head to treat insomnia and/or anxiety

Other clearances by Neurofield, Inc.

  • K240420 — NeuroField Analysis Suite (September 20, 2024)
  • K221959 — Q21 (August 31, 2023)

Other clearances for product code QJQ

  • K232253 — Modius Stress (March 27, 2024)
  • K230826 — Modius Sleep (October 27, 2023)
  • K182311 — Cervella (March 7, 2019)
  • K090052 — CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/C (May 29, 2009)
  • K070412 — ELEXOMA MEDIC (May 21, 2008)
  • K062284 — CES ULTRA (April 5, 2007)
  • K060158 — NET-2000 MICROCURRENT STIMULATOR (October 13, 2006)
  • K024377 — TRANSCRANIAL ELECTROTHERAPY STIMULATOR-A, MODEL TESA-1 (July 21, 2003)
  • K932050 — NH-2002 (June 5, 1995)
  • K903014 — ALPHA-STIM CS (May 12, 1992)