The following data is part of a premarket notification filed by Markoptic with the FDA for Improved Arthroscope.
| Device ID | K830120 |
| 510k Number | K830120 |
| Device Name: | IMPROVED ARTHROSCOPE |
| Classification | Arthroscope |
| Applicant | MARKOPTIC 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-11 |
| Decision Date | 1983-03-17 |