FDA 510(k)
FDA class 3
Substantially Equivalent
🇺🇸 United States
CILCO ANTERIOR CHAMBER LENS
K Number: K771933
·
Decision Jan 26, 1978
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
4
Applicant Total
1
Review Days
104
Basic Information
- Device Name
- CILCO ANTERIOR CHAMBER LENS
- K Number
- K771933
- Device Class
- FDA class 3
- Clearance Type
- Traditional
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- CALIFORNIA INTRAOCULAR LENS
- Date Received
- October 14, 1977
- Decision Date
- January 26, 1978
- Product Code
- HQL
- 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 |
|---|---|---|---|
| HQL | Intraocular Lens | FDA class 3 | Ophthalmic |
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