FDA 510(k) Applications Submitted by GERALD S PALECKI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121580 | 05/30/2012 | SURELASE CO2 LASER SYSTEM | CLINICON CORP. |
| K121471 | 05/18/2012 | LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS | LIGHTSCALPEL LLC |
| K992472 | 07/26/1999 | SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM | CLINICON CORP. |
| K983463 | 10/01/1998 | SURECAUT DIAMOND LASER KNIFE | CLINICON CORP. |
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