Exercise Bicycle

FDA 510(k) K926287 · Henley Intl.

Substantially Equivalent

510(k) numberK926287

Submission

Device name
Exercise Bicycle
Applicant
Henley Intl.
Sugar Land, TX, US
Received
December 14, 1992
Decision date
March 22, 1994
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

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More from Kinetic Resources, Inc.

510(k)DeviceDecision
K943449Neurological Diagnostic DevicesGXY · Traditional 11/15/1995SE
K926279Upper Body ExerciserISD · Traditional 05/05/1994SE
K926278Stair ClimberISD · Traditional 05/05/1994SE
K926314Hydra Fitness Model 311 Total PowerISD · Traditional 03/18/1994SE
K926313Computerized Testing and Exercise SystemsBXB · Traditional 02/04/1994SE
K915864Monotrode Cutaneous ElectrodeGXY · Traditional 07/21/1993SE
K922036Sonopuls 591IMG · Traditional 06/29/1993SE
K926316True-Trac, StratusJFB · Traditional 03/24/1993SE
K920983Sonopuls 590IMI · Traditional 03/09/1993SE
K922020Endomed 582LIH · Traditional 09/22/1992SE

Questions and answers

When was Exercise Bicycle cleared by the FDA?

Exercise Bicycle (K926287) received a 510(k) decision of Substantially Equivalent on March 22, 1994, 463 days after the submission was received.

What is the product code of K926287?

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