Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Dressing, Wound, Drug
510(k) Number K223359
Device Name LUOFUCON® Ag+ Foam Dressing, LUOFUCON® Ag+ Antibacterial Foam Dressing
Applicant
Huizhou Foryou Medical Devices Co., Ltd.
North Shangxia Rd. Dongjiang Hi-Tech Industry Park
Huizhou,  CN 516005
Applicant Contact Guosheng Tan
Correspondent
Huizhou Foryou Medical Devices Co., Ltd.
North Shangxia Rd. Dongjiang Hi-Tech Industry Park
Huizhou,  CN 516005
Correspondent Contact Guosheng Tan
Classification Product Code
FRO  
Date Received11/03/2022
Decision Date 12/21/2023
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
Predetermined Change
Control Plan Authorized		 No
-
-