FDA 510(k) Applications Submitted by ULTRAGUIDE LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011418 | 05/09/2001 | ULTRAGUIDE MR-GUIDE 3000 | ULTRAGUIDE LTD. |
| K022354 | 07/19/2002 | ULTRAGUIDE CTG 2000SA | ULTRAGUIDE LTD. |
| K002258 | 07/25/2000 | ULTRAGUIDE CT-GUIDE 1010 | ULTRAGUIDE LTD. |
| K013150 | 09/20/2001 | MR-GUIDE 2000 | ULTRAGUIDE LTD. |
| K023227 | 09/27/2002 | USG 2000SA | ULTRAGUIDE LTD. |
| K974432 | 11/24/1997 | ULTRAGUIDE 1000 | ULTRAGUIDE LTD. |
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