FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
D & K SUNGLASSES
K Number: K960797
·
Decision Mar 12, 1996
Classifications
1
FEI Numbers
1390
Registration Numbers
1390
Same Product Code
645
Applicant Total
3
Review Days
14
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Basic Information
- Device Name
- D & K SUNGLASSES
- K Number
- K960797
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.5850
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- D&K Stores, Inc.
- Date Received
- February 27, 1996
- Decision Date
- March 12, 1996
- Product Code
- HQY
- 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 |
|---|---|---|---|
| HQY | Sunglasses (Non-Prescription Including Photosensitive) | FDA class 1 | Ophthalmic |
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