FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇮 Finland
HAAG-STREIT FUNDUS MODULE 300
K Number: K163021
·
Decision Apr 11, 2017
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
5
Review Days
162
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Basic Information
- Device Name
- HAAG-STREIT FUNDUS MODULE 300
- K Number
- K163021
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.1120
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Optomed OY
- Date Received
- October 31, 2016
- Decision Date
- April 11, 2017
- Product Code
- HKI
- 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 |
|---|---|---|---|
| HKI | Camera, Ophthalmic, Ac-Powered | FDA class 2 | Ophthalmic |
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