K022509 is an FDA 510(k) clearance for the BRUNO ELECTRA-RIDE, MODEL SRE-2700. This device is classified as a Transport, Patient, Powered (Class II - Special Controls, product code ILK).
Submitted by Bruno Independent Living Aids, Inc. (Oconomowoc, US). The FDA issued a Cleared decision on August 13, 2002, 14 days after receiving the submission on July 30, 2002.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.5150. 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..
| 510(k) Number | K022509 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 30, 2002 |
| Decision Date | August 13, 2002 |
| Days to Decision | 14 days |
| Submission Type | Special |
| Review Panel | Physical Medicine (PM) |
| Summary | Statement |
| Product Code | ILK — Transport, Patient, Powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 890.5150 |
| Definition | 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. |