FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HANDIVIPP
K Number: K033125
·
Decision Oct 30, 2003
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
1
Review Days
30
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Basic Information
- Device Name
- HANDIVIPP
- K Number
- K033125
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Handinor USA, Inc.
- Date Received
- September 30, 2003
- Decision Date
- October 30, 2003
- 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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