The following data is part of a premarket notification filed by Feeltech Co., Ltd. with the FDA for Miracu.
Device ID | K172602 |
510k Number | K172602 |
Device Name: | Miracu |
Classification | Suture, Surgical, Absorbable, Polydioxanone |
Applicant | Feeltech Co., Ltd. 3,4 Floor Standard Factory 2-dong, 15 Jayumuyeok 2-gil Gunsan-si, KR 573-540 |
Contact | Keun-sik Kim |
Correspondent | Albert Rego Albert Rego, Ph.D., Inc. 27001 La Paz Rd, #314 Mission Viejo, CA 92691 |
Product Code | NEW |
CFR Regulation Number | 878.4840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-30 |
Decision Date | 2018-11-14 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MIRACU 90049018 not registered Live/Pending |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2020-07-13 |
MIRACU 90048987 not registered Live/Pending |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2020-07-13 |
MIRACU 88868205 not registered Live/Pending |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2020-04-10 |
MIRACU 87832960 5631265 Live/Registered |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2018-03-14 |
MIRACU 87632513 5870806 Live/Registered |
BENEV DBM Corporation 2017-10-03 |
MIRACU 87616867 5413016 Live/Registered |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2017-09-21 |
MIRACU 87616863 5413015 Live/Registered |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2017-09-21 |
MIRACU 86564584 4930712 Live/Registered |
WAYING TECHNOLOGY DEVELOPMENT CO., LIMITED 2015-03-16 |