FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VISTEK ELECTRONIC CONTROLLER
K Number: K904682
·
Decision Dec 18, 1990
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
40
Applicant Total
5
Review Days
64
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Basic Information
- Device Name
- VISTEK ELECTRONIC CONTROLLER
- K Number
- K904682
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4820
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Vistek Corp.
- Date Received
- October 15, 1990
- Decision Date
- December 18, 1990
- Product Code
- GEY
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GEY | Motor, Surgical Instrument, Ac-Powered | FDA class 1 | General, Plastic Surgery |
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