Quadruple Jogger Exerciser

FDA 510(k) K821016 · Industrial Energy Specialists, Inc.

Substantially Equivalent

510(k) numberK821016

Submission

Device name
Quadruple Jogger Exerciser
Applicant
Industrial Energy Specialists, Inc.
Mchenry, IL, US
Received
April 12, 1982
Decision date
April 26, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BXB – Exerciser, Powered
Device class
Class I (low risk)
Regulation
21 CFR 890.5380
Specialty
Physical Medicine

Other 510(k)s with product code BXB

510(k)DeviceApplicantDecision
K072887G-Trainer MedicalBXB · Traditional Alter-G, Inc.01/25/2008SE
K003272Flo-BootBXB · Traditional Discovery Group, LLC04/04/2001SE
K952975Ankle Calf Exerciser PhlebopumpBXB · Traditional Prevent Products, Inc.09/25/1996SE
K953456E-Z FlexBXB · Traditional Fluid Motion Biotechnologies, Inc.01/26/1996SE
K955106Bte CPM-20BXB · Traditional Baltimore Therapeutic Equipment Co.12/29/1995SE
K955105Bte CPM-10BXB · Traditional Baltimore Therapeutic Equipment Co.12/29/1995SE
K951028Hamex TwoBXB · Traditional Northern Orthopaedic Products, Inc.12/11/1995SE
K950755Flexmate K500BXB · Traditional Breg, Inc.10/05/1995SE
K951029Hamex OneBXB · Traditional Northern Orthopaedic Products, Inc.09/15/1995SE
K945733Aquahab, Model 120-72-101BXB · Traditional Aquarius Electronics, Inc.09/15/1995SE

Questions and answers

When was Quadruple Jogger Exerciser cleared by the FDA?

Quadruple Jogger Exerciser (K821016) received a 510(k) decision of Substantially Equivalent on April 26, 1982, 14 days after the submission was received.

What is the product code of K821016?

The FDA product code is BXB – Exerciser, Powered, a Class I (low risk) device regulated under 21 CFR 890.5380.