FDA 510(k)
FDA class 1
Substantially Equivalent
🇬🇧 United Kingdom
RGK Daily Range Wheelchairs
K Number: K200135
·
Decision Sep 10, 2020
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
1
Review Days
233
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Basic Information
- Device Name
- RGK Daily Range Wheelchairs
- K Number
- K200135
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Rgk Wheelchairs, Ltd.
- Date Received
- January 21, 2020
- Decision Date
- September 10, 2020
- Product Code
- IOR
- 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 |
|---|---|---|---|
| IOR | Wheelchair, Mechanical | FDA class 1 | Physical Medicine |
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