The following data is part of a premarket notification filed by Alcon Research, Ltd. with the FDA for Monarch Ii Iol Delivery System.
| Device ID | K001157 |
| 510k Number | K001157 |
| Device Name: | MONARCH II IOL DELIVERY SYSTEM |
| Classification | Lens, Guide, Intraocular |
| Applicant | ALCON RESEARCH, LTD. 6201 SOUTH FREEWAY Fort Worth, TX 76134 -2099 |
| Contact | Sherri J Lakota |
| Correspondent | Sherri J Lakota ALCON RESEARCH, LTD. 6201 SOUTH FREEWAY Fort Worth, TX 76134 -2099 |
| Product Code | KYB |
| CFR Regulation Number | 886.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-04-10 |
| Decision Date | 2000-06-27 |