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510(k) K911795

KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000) by Breg, Inc. — Product Code LXV

K911795 is an FDA 510(k) premarket notification submitted by Breg, Inc. for the device "KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)". The FDA issued a decision of Substantially Equivalent on November 19, 1991. The device falls under product code LXV (Apparatus, Vestibular Analysis), a Class U device. Breg, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 19, 1991
Date Received
April 22, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Vestibular Analysis
Device Class
Class U
Regulation Number
Review Panel
EN
Submission Type

Other clearances by Breg, Inc.

  • K183702 — Polar Care Wave (March 1, 2019)
  • K070402 — MODIFICATION TO POLAR CARE 500 (March 29, 2007)
  • K041714 — E-PAIN CARE (October 1, 2004)
  • K020988 — PAIN CARE 4200 (April 4, 2002)
  • K013928 — PAIN CARE 3200 (December 3, 2001)
  • K003611 — PAIN CARE MULTI-PORT CATHETER, MODEL 2000L (December 13, 2000)
  • K002073 — PAIN CARE 3000 (September 19, 2000)
  • K002321 — PAIN CARE 2000L (August 14, 2000)
  • K983454 — PAIN CARE 2000 (December 16, 1998)
  • K963596 — POLAR CARE 300 (December 4, 1996)

Other clearances for product code LXV

  • K220231 — GyroStim (April 27, 2022)
  • K200529 — Orion (August 12, 2020)
  • K192652 — TRV (May 27, 2020)
  • K183661 — ClearEdge Balance System (October 22, 2019)
  • K190735 — EQ Balance (August 16, 2019)
  • K173669 — K-D Balance (April 2, 2018)
  • K121590 — VESTIBULAR ANALYSIS APPARATUS (September 20, 2012)
  • K102364 — NYDIAG 200 (December 23, 2010)
  • K082634 — VERTIGONE BPPV GOGGLE (April 7, 2009)
  • K081602 — DIZZYFIX (September 19, 2008)

FDA data resources