510(k) K200583

Device
Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL
Applicant
Ki Mobility, LLC
510(k) number
K200583
Product code
IOR
Decision
Substantially Equivalent (SESE)
Decision date
2023-09-05
Date received
2020-03-06
Regulation
890.3850
Classification name
Wheelchair, Mechanical
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Mark Murphy
Address
5201 Woodward Dr. Stevens Point WI US 54481 54481

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code IOR#

510(k), Device, Applicant table
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