C-Max, C-Max U1, C-Max U1 160KG, C-Max U2, C-Max U2 160KG, S-Max, S-Max Aviation, S-Max Sella, S-Max Sella 160KG

FDA 510(k) K103122 · Aat Alber Antriebstechnik GmbH

Substantially Equivalent

510(k) numberK103122

Submission

Device name
C-Max, C-Max U1, C-Max U1 160KG, C-Max U2, C-Max U2 160KG, S-Max, S-Max Aviation, S-Max Sella, S-Max Sella 160KG
Applicant
Aat Alber Antriebstechnik GmbH
Texas City, TX, US
Received
October 21, 2010
Decision date
December 30, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ILK – Transport, Patient, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5150
Specialty
Physical Medicine

A powered patient transport is a motorized device intended for use in mitigating mobility impairment caused by injury or other disease by moving a person from one location or level to another, such as up and down flights of stairs (e.g., attendant-operated portable stair-climbing chairs). This generic type of device does not include motorized three-wheeled vehicles or wheelchairs.

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K111858Liftkar PTILK · Traditional Sano Transportgeraete GmbH11/04/2011SE
K093946Hoveround Hoverglide Model Hoverglide MK-2ILK · Traditional Hoveround Corp.03/22/2010SE
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More from Merits Health Products Co., Ltd.

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Questions and answers

When was C-Max, C-Max U1, C-Max U1 160KG, C-Max U2, C-Max U2 160KG, S-Max, S-Max Aviation, S-Max Sella, S-Max Sella 160KG cleared by the FDA?

C-Max, C-Max U1, C-Max U1 160KG, C-Max U2, C-Max U2 160KG, S-Max, S-Max Aviation, S-Max Sella, S-Max Sella 160KG (K103122) received a 510(k) decision of Substantially Equivalent on December 30, 2010, 70 days after the submission was received.

What is the product code of K103122?

The FDA product code is ILK – Transport, Patient, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5150.