FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AUTO ENTRY SYSTEM (MATE)
K Number: K870425
·
Decision Mar 24, 1987
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
2
Review Days
49
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Basic Information
- Device Name
- AUTO ENTRY SYSTEM (MATE)
- K Number
- K870425
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Kg Engineering, Inc.
- Date Received
- February 3, 1987
- Decision Date
- March 24, 1987
- 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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Other Clearances by Kg Engineering, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K854257 | COMBO 36 | Nov 18, 1985 | Substantially Equivalent |