FDA 510(k) Applications Submitted by PRESWEDE AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030423 | 02/10/2003 | POWERLITE 600 EP SYSTEM | PRESWEDE AB |
| K033933 | 12/19/2003 | POWERLITE 600 EX SYSTEM | PRESWEDE AB |
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