FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MULTIPLE
K Number: K933453
·
Decision Oct 13, 1993
Classifications
1
FEI Numbers
1189
Registration Numbers
1190
Same Product Code
197
Applicant Total
1
Review Days
92
Basic Information
- Device Name
- MULTIPLE
- K Number
- K933453
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.5842
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- FORTUNA OPTICAL FACTORY LTD.
- Date Received
- July 13, 1993
- Decision Date
- October 13, 1993
- Product Code
- HQZ
- 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 |
|---|---|---|---|
| HQZ | Frame, Spectacle | FDA class 1 | Ophthalmic |
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