K240843
- 510(k) number
- K240843
- Device name
- GENESIS (MS-P02-GEN)
- Applicant
- Climbing Steps, Inc. NY · US
- Product code
- ILK — Transport, Patient, Powered
- Decision date
- 2024-10-07
- Date received
- 2024-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K240843
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.