FDA 510(k) Applications Submitted by DANIEL I ANDERSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960295 | 01/22/1996 | LONG LIFE RX-12 | REXTON, INC. |
| K964451 | 11/06/1996 | PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATC | REXTON, INC. |
| K970537 | 02/12/1997 | REXTON MODEL 48 AND 49PP | REXTON, INC. |
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