The following data is part of a premarket notification filed by Kj Meditech Co., Ltd with the FDA for Kj Submerged System.
Device ID | K103810 |
510k Number | K103810 |
Device Name: | KJ SUBMERGED SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | KJ MEDITECH CO., LTD 951 STARBUCK ST. UNIT J Fullerton, CA 92833 |
Contact | Priscilla Chung |
Correspondent | Priscilla Chung KJ MEDITECH CO., LTD 951 STARBUCK ST. UNIT J Fullerton, CA 92833 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-29 |
Decision Date | 2011-09-14 |
Summary: | summary |