FDA 510(k) Applications Submitted by CURATRONIC, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080787 | 03/20/2008 | BIOMOVE 5000 SYSTEM | CURATRONIC, LTD. |
| K042650 | 09/28/2004 | BIOMOVE 3000 | CURATRONIC, LTD. |
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