Uppercycle Stationary Exercise Machines

FDA 510(k) K871494 · Engineering Dynamics Corp.

Substantially Equivalent

510(k) numberK871494

Submission

Device name
Uppercycle Stationary Exercise Machines
Applicant
Engineering Dynamics Corp.
Lowell, MA, US
Received
April 16, 1987
Decision date
May 6, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K844578Non-Magnetic Examination Table for Magnetic ResonaFPO · Traditional 05/14/1985SE
K842108Universal Examination TableGZO · Traditional 07/17/1984SE
K834098Stationary Exercise BicycleISD · Traditional 12/27/1983SE
K828313Digital Radiography Examination Table · Traditional 10/07/1982SE
K802254General Ultrasound Exam. TableIYN · Traditional 11/26/1980SE
K790545Stress Testing System, Lateral TiltingDRT · Traditional 06/06/1979SE
K790544Stress Testing System, Multi-PositionDRT · Traditional 06/05/1979SE
K790466U-MatIYX · Traditional 03/28/1979SE
K790499Multiple Pinhole Tomographic CollimoterIYX · Traditional 03/26/1979SE

Questions and answers

When was Uppercycle Stationary Exercise Machines cleared by the FDA?

Uppercycle Stationary Exercise Machines (K871494) received a 510(k) decision of Substantially Equivalent on May 6, 1987, 20 days after the submission was received.

What is the product code of K871494?

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