The following data is part of a premarket notification filed by Quanta System Spa with the FDA for Q-plus T+ Ipl Laser System.
Device ID | K123168 |
510k Number | K123168 |
Device Name: | Q-PLUS T+ IPL LASER SYSTEM |
Classification | Powered Laser Surgical Instrument |
Applicant | Quanta System SpA VIA IV NOVEMBRE, 116 Solbiate Olona, Va, IT 21058 |
Contact | Maurizio Bianchi |
Correspondent | Maurizio Bianchi Quanta System SpA VIA IV NOVEMBRE, 116 Solbiate Olona, Va, IT 21058 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-10-09 |
Decision Date | 2012-12-20 |
Summary: | summary |