FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION
K Number: K940284
·
Decision Feb 28, 1994
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
4
Review Days
55
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Basic Information
- Device Name
- MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION
- K Number
- K940284
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6320
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Meddev International Corp.
- Date Received
- January 4, 1994
- Decision Date
- February 28, 1994
- Product Code
- KZF
- Advisory Committee
- General Hospital
- 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 |
|---|---|---|---|
| KZF | Device, Medical Examination, Ac Powered | FDA class 1 | General Hospital |
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