FDA 510(k) Applications Submitted by Ngoc Linh Pham Latchman
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121612 | 06/01/2012 | ELEVATE PROLAPSE REPAIR SYSTEMS-APICAL NEEDLE PASSER SHEATH MODIFICATION | AMERICAN MEDICAL SYSTEMS |
| K180258 | 01/30/2018 | SpeediCath Standard | Coloplast |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact