FDA 510(k) Applications Submitted by ARGUS PHOTONICS GROUP
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971830 | 05/16/1997 | ACCU-PULSE CARBON DIOXIDE LASER SYSTEM | ARGUS PHOTONICS GROUP |
| K983543 | 10/09/1998 | ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM | ARGUS PHOTONICS GROUP |
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