FDA 510(k) Applications Submitted by AVITRO LLC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000632 | 02/24/2000 | 0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE | AVITRO LLC. |
| K001795 | 06/14/2000 | THE AVITRO LLC, 10 AND 100 USO UNITS/ML HEPARIN SODIUM VAFD | AVITRO LLC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact