FDA 510(k) Applications Submitted by J.HARVEY KNAUSS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972572 | 07/10/1997 | SINGLE LUMEN EMBOLECTOMY CATHETER | AMERICAN BIOMED, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact