FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HOVEROUND SE-3 POWERCHAIR
K Number: K042920
·
Decision Dec 3, 2004
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
17
Review Days
42
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Basic Information
- Device Name
- HOVEROUND SE-3 POWERCHAIR
- K Number
- K042920
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3860
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Hoveround Corp.
- Date Received
- October 22, 2004
- Decision Date
- December 3, 2004
- 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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|---|---|---|---|
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| K090108 | HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR | Mar 19, 2009 | Substantially Equivalent |
| K043069 | HOVEROUND E100 POWER CHAIR | Dec 3, 2004 | Substantially Equivalent |
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| K042033 | HOVEROUND POWER WHEELCHAIR, MODEL HD700 | Sep 29, 2004 | Substantially Equivalent |
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