FDA 510(k) Applications Submitted by LUXTEC CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970562 | 02/13/1997 | TENOSNARE | LUXTEC CORP. |
| K970642 | 02/20/1997 | TENOSCOPE | LUXTEC CORP. |
| K973193 | 08/25/1997 | LUXSCOPE | LUXTEC CORP. |
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