FDA 510(k) Applications Submitted by DUOPROSS MEDITECH CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K052445 | 09/07/2005 | DUOPROSS NEEDLE | DUOPROSS MEDITECH CORPORATION |
| K042500 | 09/14/2004 | DUOPROSS SYRINGES | DUOPROSS MEDITECH CORPORATION |
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