The following data is part of a premarket notification filed by Endo Lase, Inc. with the FDA for Flexible Liquid Light Guide.
| Device ID | K834487 |
| 510k Number | K834487 |
| Device Name: | FLEXIBLE LIQUID LIGHT GUIDE |
| Classification | Image, Illumination, Fiberoptic, For Endoscope |
| Applicant | ENDO LASE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FFS |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-13 |
| Decision Date | 1984-02-21 |