FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DOT VISUAL ACVITY TEST 2000
K Number: K833956
·
Decision Jan 4, 1984
Classifications
1
FEI Numbers
106
Registration Numbers
107
Same Product Code
31
Applicant Total
3
Review Days
49
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Basic Information
- Device Name
- DOT VISUAL ACVITY TEST 2000
- K Number
- K833956
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.1150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Good-Lite Co.
- Date Received
- November 16, 1983
- Decision Date
- January 4, 1984
- Product Code
- HOX
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HOX | Chart, Visual Acuity | FDA class 1 | Ophthalmic |
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