K223359
- 510(k) number
- K223359
- Device name
- LUOFUCON® Ag+ Foam Dressing, LUOFUCON® Ag+ Antibacterial Foam Dressing
- Applicant
- Huizhou Foryou Medical Devices Co., Ltd. CN
- Product code
- FRO — Dressing, Wound, Drug
- Decision date
- 2023-12-21
- Date received
- 2022-11-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
510(k) Summary (official FDA PDF): K223359.pdf
Official FDA record: K223359
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.