FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AUTO PERIOMETER 3000
K Number: K822580
·
Decision Sep 30, 1982
Classifications
1
FEI Numbers
66
Registration Numbers
67
Same Product Code
40
Applicant Total
4
Review Days
36
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Basic Information
- Device Name
- AUTO PERIOMETER 3000
- K Number
- K822580
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.1605
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Dicon, Inc.
- Date Received
- August 25, 1982
- Decision Date
- September 30, 1982
- Product Code
- HPT
- 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 |
|---|---|---|---|
| HPT | Perimeter, Automatic, Ac-Powered | FDA class 1 | Ophthalmic |
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