510(k) K231032

Device
AMP by Method Mobility, AMP Plus (or +) by Method Mobility
Applicant
Method Mobility
510(k) number
K231032
Product code
ITI
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-10
Date received
2023-04-11
Regulation
890.3860
Classification name
Wheelchair, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
Paul Dickie
Address
2562 N. Fordham Fresno CA US 93727 93727

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Related GUDID Devices

Primary DIBrandCompanyPublished
00199874773407AMP jsMethod Mobility, Inc.2026-05-25
00199874251073AMPMethod Mobility, Inc.2026-05-25
00199874244891AMP plusMethod Mobility, Inc.2026-05-25

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