Stepmill Exercise System

FDA 510(k) K926170 · Stairmaster Sports/Medical Products, Inc.

Substantially Equivalent

510(k) numberK926170

Submission

Device name
Stepmill Exercise System
Applicant
Stairmaster Sports/Medical Products, Inc.
Tulsa, OK, US
Received
November 23, 1992
Decision date
March 31, 1993
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

510(k)DeviceApplicantDecision
K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal…ISD · Abbreviated Lode B.V.12/21/2020SE
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
K952163David Back Clinic SystemISD · Traditional Kinetic Resources, Inc.08/12/1996SE

Questions and answers

When was Stepmill Exercise System cleared by the FDA?

Stepmill Exercise System (K926170) received a 510(k) decision of Substantially Equivalent on March 31, 1993, 128 days after the submission was received.

What is the product code of K926170?

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