FDA 510(k) Applications Submitted by RADIOMETER AMERICA INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K153712 | 12/24/2015 | VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification Kit | RADIOMETER AMERICA INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact