FDA 510(k) Applications for Medical Device Product Code "MUK"
| FDA 510(k) Number |
Applicant |
Device Name |
Decision Date |
| K020126 |
SURX, INC. |
MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM) |
03/15/2002 |
| K011190 |
SURX, INC. |
SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM) |
01/08/2002 |
| K020952 |
SURX, INC. |
SURX RF SYSTEM |
05/30/2002 |
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