FDA 510(k) Applications Submitted by DURMUS KOCH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K961980 | 05/20/1996 | BIPORE BALLOON DILATATION CATHETER | BIPORE, INC. |
| K973563 | 09/19/1997 | BIPORE BALLOON DILATATION CATHETER | BIPORE, INC. |
| K983650 | 10/16/1998 | BIPORE BALLOON DILATATION CATHETER | BIPORE, INC. |
| K964814 | 11/29/1996 | BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER | BIPORE, INC. |
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