FDA 510(k) Applications Submitted by Ortho8, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220761 | 03/15/2022 | CIRCUL8 Connect DVT Prevention Device | Ortho8, Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact