FDA 510(k) Applications Submitted by SUNMAX VIETNAM CO. LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101870 | 07/06/2010 | SUNMAX VIETNAM CO. LTD POWDER FREE WHITE NITRILE EXAMINATION GLOVE | SUNMAX VIETNAM CO. LTD |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact