FDA 510(k) Applications Submitted by LYNN LAYMAN-SPILLAR
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K955002 | 11/01/1995 | MAHURKAR 8 FR DUAL LEMEN CATHETER | QUINTON, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact