FDA 510(k) Applications Submitted by KANEKA PHARMA AMERICA LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121301 | 05/01/2012 | XPRESSWAY RX CATHETER (6F LD-VERISON) | KANEKA PHARMA AMERICA LLC |
| K192068 | 08/01/2019 | i-ED COIL | Kaneka Pharma America LLC |
| K170247 | 01/27/2017 | Lacriflow CL | KANEKA PHARMA AMERICA LLC |
| K101839 | 07/01/2010 | KANEKA PHARMA AMERICA XPRESS-WAY RX | KANEKA PHARMA AMERICA LLC |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact