The following data is part of a premarket notification filed by Innovative Surgical Products Inc. with the FDA for Lens Insertion Glide.
| Device ID | K840694 |
| 510k Number | K840694 |
| Device Name: | LENS INSERTION GLIDE |
| Classification | Lens, Guide, Intraocular |
| Applicant | INNOVATIVE SURGICAL PRODUCTS INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KYB |
| CFR Regulation Number | 886.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-16 |
| Decision Date | 1984-05-09 |