The following data is part of a premarket notification filed by Vevazz, Llc with the FDA for Vevazz Led.
Device ID | K172111 |
510k Number | K172111 |
Device Name: | Vevazz LED |
Classification | Fat Reducing Low Level Laser |
Applicant | Vevazz, LLC 3839 McKinney Ave. #251 Dallas, TX 75204 |
Contact | Jamie Fettig |
Correspondent | Jamie Fettig Vevazz, LLC 3839 McKinney Ave. #251 Dallas, TX 75204 |
Product Code | OLI |
CFR Regulation Number | 878.5400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-13 |
Decision Date | 2017-11-22 |
Summary: | summary |