The following data is part of a premarket notification filed by Medigroup with the FDA for Medigroup Lg-102 Light Guide.
| Device ID | K823293 |
| 510k Number | K823293 |
| Device Name: | MEDIGROUP LG-102 LIGHT GUIDE |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | MEDIGROUP 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-11-05 |
| Decision Date | 1983-05-05 |