FDA 510(k) Applications Submitted by LARISA GERSTEIN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050091 | 01/14/2005 | TRIPTER-X1 COMPACT DUET SP (SEPARATED PULSE) | DIREX SYSTEMS CORP. |
| K040474 | 02/24/2004 | ACCUSOFT | DIREX SYSTEMS CORP. |
| K043409 | 12/10/2004 | ACCUCHANGER | DIREX SYSTEMS CORP. |
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