FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
M.D.C. PORTA-LIFT
K Number: K901793
·
Decision May 24, 1990
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
28
Applicant Total
2
Review Days
35
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Basic Information
- Device Name
- M.D.C. PORTA-LIFT
- K Number
- K901793
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3930
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Metal Dynamics Corp.
- Date Received
- April 19, 1990
- Decision Date
- May 24, 1990
- Product Code
- ING
- 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 |
|---|---|---|---|
| ING | Elevator, Wheelchair, Portable | FDA class 2 | Physical Medicine |
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Other Clearances by Metal Dynamics Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K901794 | AIR CUSHIONED AUTO WHEELCHAIR LIFT ACL-200/AG-Z2 | May 7, 1990 | Substantially Equivalent |