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 |