FDA 510(k)
FDA class 2
Substantially Equivalent
🇦🇺 Australia
XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)
K Number: K233877
·
Decision Mar 4, 2024
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
4
Review Days
88
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Basic Information
- Device Name
- XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)
- K Number
- K233877
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3860
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Magic Mobility
- Date Received
- December 7, 2023
- Decision Date
- March 4, 2024
- Product Code
- ITI
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ITI | Wheelchair, Powered | FDA class 2 | Physical Medicine |
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