FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POWER EXAMINATION TABLE MODEL # 405
K Number: K894144
·
Decision Aug 28, 1989
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
13
Applicant Total
31
Review Days
76
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Basic Information
- Device Name
- POWER EXAMINATION TABLE MODEL # 405
- K Number
- K894144
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4960
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Midmark Corp.
- Date Received
- June 13, 1989
- Decision Date
- August 28, 1989
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LGX), ordered by most recent decision date.
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