FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PORTABLE LIFT SEAT
K Number: K923804
·
Decision Feb 12, 1993
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
52
Applicant Total
1
Review Days
198
Basic Information
- Device Name
- PORTABLE LIFT SEAT
- K Number
- K923804
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3110
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- FRANK H. SPECKHART, P.E.
- Date Received
- July 29, 1992
- Decision Date
- February 12, 1993
- Product Code
- INO
- 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 |
|---|---|---|---|
| INO | Chair, Positioning, Electric | FDA class 2 | Physical Medicine |
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