FDA 510(k) Applications Submitted by KAREN BROWNE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K021906 | 06/10/2002 | QUINTON Q-CATH, MODEL 000460 | QUINTON, INC. |
| K041607 | 06/15/2004 | QUINTON Q-TE; RMS | QUINTON CARDIOLOGY, INC. |
| K032038 | 07/01/2003 | PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601 | QUINTON, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact