FDA 510(k) Applications Submitted by DAN DILLION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K122050 | 07/12/2012 | CPRMETER CPR FEEDBACK DEVICE | LAERDAL MEDICAL A/S |
| K974788 | 12/22/1997 | CRE(TM) BALLOON DILATATION CATHETER | BOSTON SCIENTIFIC CORP. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact