The following data is part of a premarket notification filed by Imedicom Co., Ltd. with the FDA for Medinaut Plus.
| Device ID | K182287 |
| 510k Number | K182287 |
| Device Name: | MEDINAUT Plus |
| Classification | Arthroscope |
| Applicant | Imedicom Co., Ltd. #612, 172, LS-ro Gunpo-si, KR 435824 |
| Contact | Bonggu Ha |
| Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 690 Roosevelt Irvine, CA 92620 |
| Product Code | HRX |
| Subsequent Product Code | HXG |
| Subsequent Product Code | NDN |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-23 |
| Decision Date | 2019-04-06 |