FDA 510(k) Applications Submitted by Babu Periasamy
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171808 | 06/19/2017 | TDM Plate and Screw System | TDM Co. Ltd. |
| K123532 | 11/16/2012 | OCELOT PIXL CATHETER | AVINGER, INC. |
| K143412 | 11/28/2014 | ADROIT Guiding Catheter | CORDIS CORPORATION |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact