The following data is part of a premarket notification filed by Quanta System Spa with the FDA for Litho 150, Cyber Ho 150.
Device ID | K201455 |
510k Number | K201455 |
Device Name: | Litho 150, Cyber Ho 150 |
Classification | Powered Laser Surgical Instrument |
Applicant | Quanta System Spa Via Acquedotto 109 Samarate (va), IT 21017 |
Contact | Francesco Dell'antonio |
Correspondent | Francesco Dell'antonio Quanta System Spa Via Acquedotto 109 Samarate (va), IT 21017 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-06-01 |
Decision Date | 2020-06-30 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08059173391738 | K201455 | 000 |