FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MEDALIST EXAMINATION TABLE
K Number: K883680
·
Decision Oct 4, 1988
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
13
Applicant Total
5
Review Days
36
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Basic Information
- Device Name
- MEDALIST EXAMINATION TABLE
- K Number
- K883680
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4960
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Hamilton Industries, Inc.
- Date Received
- August 29, 1988
- Decision Date
- October 4, 1988
- Product Code
- LGX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| LGX | Table, Examination, Medical, Powered | FDA class 1 | General, Plastic Surgery |
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