The following data is part of a premarket notification filed by California Intraocular Lens with the FDA for Cilco Anterior Chamber Lens.
| Device ID | K771933 |
| 510k Number | K771933 |
| Device Name: | CILCO ANTERIOR CHAMBER LENS |
| Classification | Intraocular Lens |
| Applicant | CALIFORNIA INTRAOCULAR LENS 803 N. Front St. Suite 3 McHenry, IL 60050 |
| Product Code | HQL |
| CFR Regulation Number | 886.3600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-10-14 |
| Decision Date | 1978-01-26 |