FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WILLIAMS ADVANTAGE ELEVATION TABLE
K Number: K922719
·
Decision Aug 7, 1992
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
4
Review Days
63
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Basic Information
- Device Name
- WILLIAMS ADVANTAGE ELEVATION TABLE
- K Number
- K922719
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3760
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Williams Manufacturing Co.
- Date Received
- June 5, 1992
- Decision Date
- August 7, 1992
- Product Code
- INQ
- 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 |
|---|---|---|---|
| INQ | Table, Powered | FDA class 1 | Physical Medicine |
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