FDA 510(k) Applications Submitted by MEDIREX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960198 | 01/16/1996 | DIGISCOPE RX-2 | MEDIREX, INC. |
| K964327 | 10/30/1996 | IPU RX-2 | MEDIREX, INC. |
| K965013 | 12/16/1996 | DIGISCOPE RX-2 (9 OPTION) | MEDIREX, INC. |
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