David Back Clinic System

FDA 510(k) K952163 · Kinetic Resources, Inc.

Substantially Equivalent

510(k) numberK952163

Submission

Device name
David Back Clinic System
Applicant
Kinetic Resources, Inc.
Fort Worth, TX, US
Received
May 8, 1995
Decision date
August 12, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
ISD – Exerciser, Measuring
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5360
Specialty
Physical Medicine

Other 510(k)s with product code ISD

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K183296REAL Immersive SystemISD · Traditional Penumbra, Inc.03/18/2019SE
K143512ActiSpec Activity MonitorISD · Traditional Sleep Modus, Inc.08/26/2015SE
K112121Ergoselect/GeISD · Traditional Ergoline GmbH10/31/2012SE
K080545ActitrainerISD · Traditional Actigraph, LLC07/24/2008SE
K053078Ergoselect 100 K/P, Ergoselect 200 K/PISD · Traditional Ergoline GmbH04/27/2006SE
K990866Quinton Medtrack CR Plus TreadmillISD · Traditional Quinton, Inc.04/29/1999SE
K990813RehcorISD · Traditional Electromed Corp.04/12/1999SE
K962855ULE-2, MULE-2, Hand Accessory KitISD · Traditional Penny and Giles Biometrics , Ltd.12/11/1996SE
K941033Physio HabISD · Traditional Longo Industries02/27/1995SE

Questions and answers

When was David Back Clinic System cleared by the FDA?

David Back Clinic System (K952163) received a 510(k) decision of Substantially Equivalent on August 12, 1996, 462 days after the submission was received.

What is the product code of K952163?

The FDA product code is ISD – Exerciser, Measuring, a Class II (moderate risk) device regulated under 21 CFR 890.5360.