FDA 510(k) Applications Submitted by LUMEX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K962123 | 05/31/1996 | AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM | LUMEX, INC. |
| K963674 | 09/13/1996 | LUMEX AIR | LUMEX, INC. |
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