The following data is part of a premarket notification filed by Quantel Medical with the FDA for Vitra Multispot.
Device ID | K122251 |
510k Number | K122251 |
Device Name: | VITRA MULTISPOT |
Classification | Powered Laser Surgical Instrument |
Applicant | QUANTEL MEDICAL 5 TIMBER LANE North Reading, MA 01864 |
Contact | Maureen O'connell |
Correspondent | Maureen O'connell QUANTEL MEDICAL 5 TIMBER LANE North Reading, MA 01864 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-07-27 |
Decision Date | 2013-01-24 |
Summary: | summary |