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 |