CILCO ANTERIOR CHAMBER LENS
FDA 510(k) clearance K771933 · decided 1978-01-26
Clearance details
- K-number
- K771933
- Device name
- CILCO ANTERIOR CHAMBER LENS
- Applicant
- California Intraocular Lens
- Decision
- Substantially Equivalent
- Date received
- 1977-10-14
- Decision date
- 1978-01-26
- Days to decision
- 104 days
- Clearance type
- Traditional
- Product code
- HQL
- Device class
- 3
- Regulation number
- 886.3600
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| CHIROFLEX II LENS MICROSERT(TM) (K914311) | Chiron Ophthalmics | 1992-01-27 |
| SOFTRANS INJECTOR (K913626) | Staar Surgical Co. | 1991-12-18 |
| NIDEK DIGITAL KERATOMETER (K842892) | Nidek, Inc. | 1984-10-05 |
| AMER. MEDICAL OPTICS DIGITAL KERATO- (K842504) | American Medical Optics | 1984-10-01 |
Recalls involving this device
No recalls on record reference this clearance.