FDA 510(k) Applications Submitted by Chungwoo CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222709 | 09/08/2022 | Retraction, CWM-910T, APOLEX Tite | Chungwoo CO., LTD. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact