Equitest

FDA 510(k) K851744 · Neurocom International, Inc.

Substantially Equivalent

510(k) numberK851744

Submission

Device name
Equitest
Applicant
Neurocom International, Inc.
Portland, OR, US
Received
April 29, 1985
Decision date
August 5, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LXV – Apparatus, Vestibular Analysis
Device class
Unclassified

Other 510(k)s with product code LXV

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K183661ClearEdge Balance SystemLXV · Traditional Quadrant Biosciences10/22/2019SE
K190735EQ BalanceLXV · Traditional Upright Science, Inc.08/16/2019SE
K173669K-D BalanceLXV · Traditional King-Devick Technologies, Inc.04/02/2018SE
K121590Vestibular Analysis ApparatusLXV · Traditional Capacity Sports, LLC09/20/2012SE
K102364Nydiag 200LXV · Traditional Interacoustics A/S12/23/2010SE
K082634Vertigone BPPV GoggleLXV · Traditional Vertigone, Inc.04/07/2009SE
K081602DizzyfixLXV · Traditional Clearwater Clinical Limited09/19/2008SE

More from Clearwater Clinical Limited

510(k)DeviceDecision
K946229Balance ManagerKHX · Traditional 08/04/1995SE
K901732Emg Accessory for PosturographyIKN · Traditional 09/10/1991SE
K871652Neurocom Pressure Test SystemETY · Traditional 07/16/1987SE
K863443Dual ForceplateKHX · Traditional 09/17/1986SE

Questions and answers

When was Equitest cleared by the FDA?

Equitest (K851744) received a 510(k) decision of Substantially Equivalent on August 5, 1985, 98 days after the submission was received.

What is the product code of K851744?

The FDA product code is LXV – Apparatus, Vestibular Analysis, a Unclassified device.