FDA 510(k)
FDA class 1
Substantially Equivalent
🇨🇦 Canada
KINESETHETIC SEATING SYSTEM/WHEELCHAIR
K Number: K861754
·
Decision May 23, 1986
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
3
Review Days
17
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Basic Information
- Device Name
- KINESETHETIC SEATING SYSTEM/WHEELCHAIR
- K Number
- K861754
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3920
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Special Health Systems, Ltd.
- Date Received
- May 6, 1986
- Decision Date
- May 23, 1986
- Product Code
- KNN
- 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 |
|---|---|---|---|
| KNN | Components, Wheelchair | FDA class 1 | Physical Medicine |
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