FDA 510(k) Applications Submitted by ANNE BUTEYN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972962 | 08/11/1997 | 3M CDI BLOOD PARAMETER MONITORING SYSTEM 500 | 3M COMPANY |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact