FDA 510(k) Applications Submitted by ENDOCROSS, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K092174 | 07/21/2009 | ENABLER-P CATHETER SYSTEM, MODEL 3000 | ENDOCROSS, LTD. |
| K083833 | 12/23/2008 | ENABLER-P CATHETER, 1000 PART NUMBER:1160 | ENDOCROSS, LTD. |
| K082339 | 08/14/2008 | ENABLER-P SUPPORT CATHETER | ENDOCROSS, LTD. |
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