510(k) K130864
K130864 is an FDA 510(k) premarket notification submitted by Aat Alber Antriebstechnik GmbH for the device "C-MAX+ (PLUS)". The FDA issued a decision of Substantially Equivalent on February 6, 2014. The device falls under product code ILK (Transport, Patient, Powered), a Class II device regulated under 21 CFR 890.5150. Aat Alber Antriebstechnik GmbH has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 6, 2014
- Date Received
- March 28, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transport, Patient, Powered
- Device Class
- Class II
- Regulation Number
- 890.5150
- Review Panel
- PM
- Submission Type
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.